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A Minnesota appeals court recently affirmed a $6.7 million jury award to a maintenance worker for injuries caused by a truck driver who drove too fast over a hose. Though unusual, the case serves as a cautionary tale for any truck driver.

The Minneapolis worker was clearing a sewer cave-in in the middle of a busy urban street, with traffic cones directing traffic to the outer lanes. He was using a power washer connected to a hose that crossed an active lane of traffic to connect to a fire hydrant. The posted speed limit was 30 mph.

The driver of a large beverage truck said he didn’t notice the work zone until he was about 30 feet away. When he drove over the hose, it became entangled in the truck’s rear axle and tore away from the hydrant. A heavy metal object — either the end of the hose or a manhole cover that was lying on the hose — went airborne and struck the maintenance worker’s foot, partially severing it.

Speed and the ‘water hammer’ effect

At trial, the speed of the truck became a key issue. The driver said he was going 20 mph, a passenger said it was 30 mph, and an expert witness gave a “conservative estimate” of between 29.9 and 36.4 mph.

The exact speed may not have been a key factor except for the pressurized hose. An expert in fluid science testified that “the only way” the hose could have become entangled was for the front wheels to cause a “water hammer” or “pressure wave” that made the hose leap into the air and remain there long enough to catch the rear axle.

Getting caught in the axle was only possible if the truck was moving fast enough to travel over 21 feet in about 0.3 seconds, or between 30 and 40 mph.

Ultimately, the jury found the driver negligent for speeding in a work zone and awarded the maintenance worker $6.73 million in damages.

Do your drivers know what to do?

At the trial, a trucking expert testified that large commercial trucks need to be “hypercautious” in work zones — something most drivers already know — but also slow down when driving across hoses. In fact, the expert recommends that drivers reduce their speed to about 10 mph before driving over a hose.

Not only can a slow speed prevent the hose from jumping into the air but also prevent it from getting tangled in the vehicle, which could lead to all sorts of mechanical and safety problems. A slow speed also gives the driver time to react to such an event.

Remind your drivers to always be alert to work zones, slow down well in advance, and be extra cautious (and slow) when crossing over a hose.

Key to remember: A recent $6.7 million jury award serves as a reminder of why speed is a critical factor when driving through work zones — and when crossing hoses.

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Most Recent Highlights In Environmental

MACT emission standards: 7 questions answered
2026-05-14T05:00:00Z

MACT emission standards: 7 questions answered

Standards are more than just suggestions when it comes to environmental regulations; they define the minimum level of performance that must be achieved and, as a result, determine who complies and who doesn’t. For industrial facilities that release air toxics, emission standards are foundational to compliance.

The Environmental Protection Agency (EPA) controls the release of more than 180 air toxics, known as hazardous air pollutants (HAPs), from industrial sources (such as factories and refineries) through the National Emission Standards for Hazardous Air Pollutants (NESHAP) program. For major sources, EPA develops maximum achievable control technology (MACT) standards to reduce HAP emissions.

Understanding the basics of MACT standards can help you navigate the requirements specific to your facility. Here’s what you need to know.

What’s a MACT standard?

A MACT standard refers to the specific technology-based requirements set by EPA to control HAP emissions from major sources in a specific industrial source category. The agency bases the standards on the emission levels already being achieved with existing control technologies by the best-controlled and lowest-emitting facilities in an industry.

What’s a MACT floor?

MACT floors are the minimum control levels that regulated facilities must meet. EPA sets MACT floors differently for new and existing facilities:

  • The MACT floors for new facilities must be at least as stringent as the emission control achieved by the best-controlled similar source.
  • The MACT floors for existing facilities (which may be less stringent than the floors for new sources) have to be at least as strict as the average emission limitation achieved by either:
    • The top-performing 12 percent of sources in a category or subcategory with 30 or more sources, or
    • The top-performing 5 sources in a category or subcategory with fewer than 30 sources.

Keep in mind that EPA may establish requirements stricter than the MACT floor, known as “beyond-the-floor” standards.

What types of facilities are subject to MACT standards?

MACT standards generally apply to major sources of HAP emissions. A facility is considered a major source if it emits or has the potential to emit:

  • 10 tons per year (tpy) of any one HAP, or
  • 25 tpy of any combination of HAPs.

How are MACT standards organized?

EPA develops MACT standards by industry sector and publishes them as part of the NESHAP regulations. Most of the rules appear under 40 CFR Part 63, organized by subparts based on source category. Facilities must identify their source category to determine which NESHAP subpart applies.

A limited number of the rules are found under Part 61, organized by subparts based on specific HAPs (such as vinyl chloride) or activities (like asbestos demolition). Facilities need to confirm whether any of the NESHAPs for specific HAPs or activities apply.

How are MACT standards enforced?

The air permitting authority (usually a state or local air agency) incorporates applicable NESHAP requirements, including MACT standards, into a facility’s Title V operating permit.

What do MACT standards cover?

MACT standards can include a combination of measures, methods, processes, systems, and techniques to reduce or eliminate HAP emissions. Examples include:

  • Conducting process changes;
  • Substituting materials;
  • Enclosing systems or processes; and
  • Collecting, capturing, and/or treating HAP releases from emission points.

MACT standards may also contain design, equipment, work practice, and operation requirements.

Can MACT standards change?

Yes. The Clean Air Act requires EPA to evaluate MACT standards every 8 years (known as a risk and technology review). The agency will revise MACT standards when it determines improvements in technologies, practices, processes, or other emission-reduction methods warrant revisions.

Real-world example

Let’s take a look at the NESHAP for Polyether Polyols (PEPO) Production (PEPO NESHAP), recently updated in March 2026.

The MACT standards that apply to the PEPO NESHAP (Part 63 Subpart PPP) include:

  • Emission limits for process vents;
  • Equipment and work practice requirements for storage vessels, wastewater, and equipment leaks; and
  • Work practice standards for heat exchange systems.

EPA concluded that improvements in controls warranted updates to specific MACT standards in the PEPO NESHAP, including for heat exchange systems. Specifically, the revised rule requires owners and operators of existing and new heat exchange systems in organic HAP service to:

  • Conduct quarterly monitoring using the Modified El Paso Method (also known as the Air Stripping Method), and
  • Repair leaks of total strippable hydrocarbon concentration (as methane) in the stripping gas of 6.2 parts per million by volume or greater.

The agency found that the Modified El Paso Method is more effective at identifying leaks, and it measures more compounds than previously required methods. As a result, this revised MACT standard will further reduce HAP emissions from heat exchange systems.

Key to remember: EPA controls hazardous air pollutant emissions from major sources through MACT standards based on the emission levels already achieved by the best-controlled facilities in an industry.

EHS Monthly Round Up - April 2026

EHS Monthly Round Up - April 2026

In this April 2026 roundup video, we’ll review the most impactful environmental health and safety news.

Hi everyone! Welcome to the monthly news roundup video, where we’ll review the most impactful environmental health and safety news. Let’s take a look at what happened over the past month.

OSHA revised its National Emphasis Program on heat-related hazards. Going forward, the agency will prioritize inspections in 55 high-risk industries in indoor and outdoor work settings. The program remains in effect for 5 years from its April 10 effective date.

An OSHA proposed rule seeks to eliminate the November 18, 2036, deadline in the Walking-Working Surfaces standard that would require all fixed ladders extending more than 24 feet above a lower level to be equipped with personal fall arrest systems or ladder safety systems. OSHA also seeks feedback on nine specific questions related to the proposal, with comments due on June 5.

On April 17, OSHA revoked its House Falls in Marine Terminals standard at 1917.41. The agency said that because most cargo has been containerized and is moved by cranes, the standard is no longer necessary to protect employees.

Turning to environmental news, an EPA final rule further delays the submission period for the one-time PFAS report required of manufacturers. It pushes the start of the submission period to either 60 days after the effective date of a future final rule updating the PFAS Reporting Rule or January 31, 2027, whichever comes first.

An EPA final rule makes technical changes to the emission standards established in March 2024 for crude oil and natural gas facilities. The changes take effect June 8.

EPA published the draft 6th Contaminant Candidate List for the next group of contaminants to be considered for regulation under the Safe Drinking Water Act. The proposed list designates microplastics and pharmaceuticals as priority contaminant groups for the first time.

And finally, EPA plans to make significant changes to coal combustion residuals requirements. A proposed rule published April 13 would revise the regulations governing the disposal of coal combustion residuals in landfills and surface impoundments, as well as the beneficial use of coal combustion residuals.

Thanks for tuning in to the monthly news roundup. We’ll see you next month!

EHS Monthly Round Up - February 2026

EHS Monthly Round Up - February 2026

In this Februrary 2026 roundup video, we'll discuss the most impactful environmental health and safety news.

Hi everyone! Welcome to the monthly news roundup video, where we’ll review the most impactful environmental health and safety news. Let’s take a look at what happened over the past month.

Fatal work injuries fell 4 percent in 2024, largely due to a decline in workplace drug- and alcohol-related overdoses. According to the Bureau of Labor Statistics, overdose fatalities fell from 512 in 2023 to 410 in 2024. Across all types of workplace incidents, there were 5,070 fatal work injuries in 2024, compared to 5,283 in 2023. Transportation incidents continue to be the most frequent type of fatal event, accounting for over 38 percent of all occupational fatalities in 2024.

OSHA is fast-tracking a proposal to remove the 2036 obligation to upgrade fall protection systems on fixed ladders that extend over 24 feet. This follows an industry petition from major chemical and petroleum industry groups, which argue the provision is unjustified, costly, and not supported by the rulemaking record. OSHA frames the upcoming proposed action as deregulatory, allowing employers to update fixed ladders at the end of their service lives. We’ll provide updates as more information becomes available.

As OSHA leans into “deregulatory” actions, lawmakers are moving to pressure the agency to issue “regulatory” rulemaking to protect American workers. The latest legislative wave of bills aims to fill regulatory gaps, tackle emerging hazards, expand OSHA authority, and raise penalties. Topics addressed by these bills include musculoskeletal disorders, heat stress, infectious diseases, wildfire smoke, and workplace violence.

In a recently issued letter of interpretation, OSHA states that a burn injury caused by a personal lithium-ion battery fire is work related if it occurs in the workplace during assigned working hours. The letter details an incident where an employee was burned when their rechargeable lithium-ion batteries for e-cigarettes sparked a fire after coming into contact with a key used for work.

A new report from the Department of Labor Office of Inspector General concludes that OSHA struggles to meet its mission, particularly in high-risk industries like healthcare, construction, and manufacturing. Several pages point to OSHA’s difficulties in effectively enforcing annual injury and illness reporting requirements, reaching the nation’s high-risk worksites for inspection, and addressing workplace violence by regulatory or other action.

Turning to environmental news, EPA extended the deadlines for Facility Evaluation Reports and related requirements for coal combustion residuals facilities. In most instances, the deadlines have been moved one or two years out.

And finally, EPA announced a final rule eliminating the 2009 Endangerment Finding and related greenhouse gas emission requirements for on-highway vehicles and vehicle engines. When the final rule takes effect, manufacturers and importers of new motor vehicles and motor vehicle engines will no longer have to measure, report, certify, or comply with federal greenhouse gas emission standards.

Thanks for tuning in to the monthly news roundup. We’ll see you next month!

EHS Monthly Round Up - March 2026

EHS Monthly Round Up - March 2026

In this March 2026 roundup video, we'll review the most impactful environmental health and safety news.

Hi everyone! Welcome to the monthly news roundup video, where we’ll review the most impactful environmental health and safety news. Let’s take a look at what happened over the past month.

OSHA released an updated Job Safety and Health poster. Employers can use either the revised version or the older one, but the poster must be displayed in a conspicuous place where workers can easily see it.

OSHA recently removed a link from its Data topic webpage that displayed a list of “high-penalty cases” at or over $40,000 since 2015. The agency says it discontinued and removed it in December. The data is frozen and archived elsewhere.

OSHA published two new resources as part of its newly launched Safety Champions Program. The fact sheet provides an overview of how the program works, eligibility criteria, and key benefits. The step-by-step guide helps businesses navigate the core elements of OSHA’s Recommended Practices for Safety and Health Programs.

Several forces are nudging OSHA to address a number of workplace hazards and high-hazard industries. This comes from other agencies, safety organizations, watchdogs, legislative proposals, and persistent injury/fatality data. Among the hazards are combustible dust; first aid; personal protective equipment; and workplace violence. How all this translates into new regulations, guidance, programmed inspections, or other initiatives remains to be seen.

Turning to environmental news, EPA issued a proposed rule to require waste handlers to use electronic manifests to track all RCRA hazardous waste shipments. Stakeholders have until May 4 to comment on the proposal.

On March 10, EPA finalized stronger emission limits for new and existing large municipal waste combustors and made other changes to related standards.

And finally, EPA temporarily extended coverage under the 2021 Multi-Sector General Permit for industrial stormwater discharges until the agency issues a new general permit. The permit expired February 28 and remains in effect for facilities previously covered. EPA won’t take enforcement action against new facilities for unpermitted stormwater discharges if the facilities meet specific conditions.

Thanks for tuning in to the monthly news roundup. We’ll see you next month!

EHS Monthly Round Up - January 2026

EHS Monthly Round Up - January 2026

In this January 2026 roundup video, we'll review the most impactful environmental health and safety news.

Hi everyone! Welcome to the monthly news roundup video, where we’ll review the most impactful environmental health and safety news. Let’s take a look at what happened over the past month.

Chemical manufacturers, importers, distributors, and employers will have an extra four months to comply with the provisions of OSHA’s revised Hazard Communication standard. When the rule was revised in 2024, it contained staggered compliance dates for those who classify or use chemical substances and mixtures. The first compliance date is now May 19 rather than January 19 of 2026.

On January 8, OSHA issued further technical corrections to its Hazard Communication final rule. An initial set of corrections was published in October 2024, and OSHA continued to review the standard for errors. The agency said these corrections should reduce confusion during the chemical classification process and prevent errors on labels and safety data sheets.

In 2024, private industry employers reported 2.5 million nonfatal workplace injuries and illnesses, according to the Bureau of Labor Statistics. This is down 3.1 percent from 2023 and largely due to a decrease in respiratory illnesses. The greatest number of cases involving days away from work, job restriction, or transfer were caused by overexertion, repetitive motion, and bodily conditions, followed by contact incidents.

Registration is open for OSHA’s Safety Champions Program, which is designed to help employers develop and implement effective safety and health programs. Participants can work at their own pace through Introductory, Intermediate, and Advanced levels.

Turning to environmental news, on January 9, EPA withdrew its direct final rule on SDS/Tier II reporting tied to OSHA HazCom, before it had a chance to take effect. The direct final rule was published back on November 17, 2025, and was intended to relax the Tier II and safety data sheet reporting requirements and align with OSHA’s HazCom standard. EPA said it plans to write a new rule addressing all public comments.

And finally, EPA published a final rule that changes certain requirements for wastewater discharges from coal-fired steam electric power plants. It applies to the deadlines established by the preceding rule finalized in 2024.

Thanks for tuning in to the monthly news roundup. We’ll see you next month!

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Most Recent Highlights In Transportation

EPA postpones compliance for TCE uses with TSCA Section 6(g) exemptions
2026-05-07T05:00:00Z

EPA postpones compliance for TCE uses with TSCA Section 6(g) exemptions

On May 5, 2026, the Environmental Protection Agency (EPA) published a final rule postponing the effective date of compliance requirements for trichloroethylene (TCE) uses with Toxic Substances Control Act (TSCA) Section 6(g) exemptions until judicial review is concluded.

Who’s impacted?

The delay applies to the conditions imposed on each TSCA Section 6(g) exemption at 40 CFR 751.325, including the Workplace Chemical Protection Program requirements at 751.315.

Since the compliance requirements haven’t taken effect, facilities that use TCE with TSCA Section 6(g) exemptions don’t have to comply with the provisions yet.

Why the delay?

In December 2024, EPA released the final TCE rule (2024 TCE rule). The rule ultimately bans all uses of TCE, but it allows uses with TSCA Section 6(g) exemptions to continue for a limited time as long as facilities comply with strict workplace controls. Currently, the 2024 TCE rule is under judicial review. EPA has delayed the effective date of the requirements for TCE uses with TSCA Section 6(g) exemptions until the judicial challenges to the 2024 TCE rule are resolved.

If you have a sense of déjà vu, it’s for a good reason. This is the fifth time the agency has delayed the compliance requirements for TSCA Section 6(g) exemptions. However, EPA’s previous postponements established specific dates for the provisions to take effect, but this rule doesn’t.

Key to remember: EPA has delayed the compliance requirements for TCE uses with TSCA Section 6(g) exemptions until judicial review is concluded.

2026-05-04T05:00:00Z

Wisconsin adds requirements to federal lead and copper drinking water rule

Effective date: May 1, 2026

This applies to: Public water systems

Description of change: The Wisconsin Department of Natural Resources (department) finalized amendments to align state regulations with the Environmental Protection Agency’s (EPA’s) updated lead and copper control requirements for drinking water. While most of the amendments conform to federal standards, the state has additional standards. The department also:

  • Requires community water systems to make four contact attempts (two more than federal requirements) by two different means for elementary schools and childcare facilities to schedule lead monitoring,
  • Requires public water systems on reduced annual monitoring to analyze and report the same number of sample results for copper and lead (instead of the federal requirements that only half of the copper samples are analyzed),
  • Requires public water systems undergoing temporary treatment or source water changes (unregulated by EPA) for more than 30 days to notify the department 10 days before the planned change or as soon as possible for an unplanned emergency change,
  • Requires groundwater system water suppliers that request to limit their entry point sampling to obtain prior approval from the department,
  • Requires water suppliers that provide point-of-use treatment devices for the corrosion control treatment compliance flexibility option to submit a written plan to the department (not required by the federal rule),
  • Grants the department the authority to require analysis of total and dissolved lead during distribution system and site assessments where the federal rule doesn’t provide this authority to the state,
  • Requires water suppliers that request to invalidate a reported sample result to provide substantial evidence that the sample meets one of the invalidation criteria in the rule, and
  • Combines the lead and copper monitoring waivers into one waiver and requires public water systems to complete at least two 6-month rounds of standard tap water monitoring (for which the federal rule only requires one 6-month round).
2026-05-04T05:00:00Z

District of Columbia updates odor control permit rules

Effective date: April 10, 2026

This applies to: Entities required to obtain an operating air permit under Nuisance Odor Regulations

Description of change: The District of Columbia’s Department of Energy and Environment (DOEE) finalized a rulemaking that allows sources of nuisance odors to implement odor controls before obtaining an operating air permit under 20 DCMR Section 200.

To qualify, an entity must obtain from the DOEE written approval of the controls in the Odor Control Plan (OCP) decision letter. Additionally, the source must apply for an operating permit under 200.2 within 60 days of receiving an OCP decision letter.

Related state info: Clean air operating permits state comparison

2026-05-04T05:00:00Z

California permanently adopts emergency vehicle rules

Effective date: April 1, 2026

This applies to: New vehicle and engine manufacturers

Description of change: The California Air Resources Board (CARB) permanently adopted the Emergency Vehicle Emissions Regulations, which CARB adopted in 2025 as a temporary measure.

The rule reverts the emission standards and requirements for vehicle and engine manufacturers to the regulations in effect before the adoption of:

  • Advanced Clean Cars II (ACC II), and
  • Heavy-Duty Engine and Vehicle Omnibus Low NOx (Omnibus).

CARB allows manufacturers to comply with ACC II and Omnibus requirements voluntarily.

In 2025, the Environmental Protection Agency revoked CARB’s waivers to implement the ACC II, Omnibus, and Advanced Clean Trucks rules.

Hazardous waste manifests: Hybrid vs. fully electronic
2026-04-28T05:00:00Z

Hazardous waste manifests: Hybrid vs. fully electronic

More industries are embracing the exclusive use of electronic platforms. For example, digital payments are replacing cash, news sites are going fully online, and cloud storage is eclipsing external computer storage. And, based on recent proposed rulemaking, hazardous waste manifests may join the list.

The Environmental Protection Agency (EPA) proposed the Paper Manifest Sunset Rule in March 2026, planning to shift to electronic-only manifests for tracking hazardous waste that’s regulated by the Resource Conservation and Recovery Act (RCRA).

If the proposed rule is finalized, regulated entities will have to track all hazardous waste shipments electronically. Specifically, generators, transporters, and receiving facilities could only use hybrid or fully electronic manifests on the Hazardous Waste Electronic Manifest System (e-Manifest).

So, what are the differences between hybrid and fully electronic manifests? Let’s compare the distinctions and explore some of the benefits that electronic manifests can offer.

What’s a hybrid manifest?

EPA initially established the hybrid manifest for generators that couldn’t fully participate in electronic manifests when the e-Manifest launched in 2018. The hybrid manifest combines paper and electronic manifests, allowing generators that aren’t registered in e-Manifest or don’t have an EPA identification (ID) number to sign printed copies of electronic manifests.

Here’s the general hybrid manifest process:

  • The first transporter initiates an electronic manifest in e-Manifest. A hard copy of the electronic manifest is printed out, and the generator and initial transporter sign the paper copy.
  • The generator keeps a signed paper copy on-site. The transporter keeps a signed paper copy with the shipment until it’s delivered to the receiving facility.
  • From that point forward, the initial transporter and all subsequent waste handlers track the shipment in e-Manifest (using electronic signatures and electronic transmissions).
  • The manifest is complete when the receiving facility or exporter electronically signs it on e-Manifest.

What’s a fully electronic manifest?

The fully electronic manifest is tracked completely online. All handlers — generators, transporters, and receiving facilities or exporters — must have an EPA ID number and be registered in e-Manifest to use the fully electronic manifest.

The entire process is conducted on e-Manifest:

  • The manifest is created electronically in e-Manifest.
  • All handlers electronically sign the manifest in e-Manifest.
  • The manifest is complete when the receiving facility or exporter electronically signs it on e-Manifest.

What benefits do electronic manifests offer?

Regardless of whether EPA’s rule is finalized as is, electronic manifests offer hazardous waste handlers a range of benefits. Consider the following potential perks.

Compliance with existing regulations

Many handlers are already required to embrace electronic manifesting. In July 2024, EPA finalized the e-Manifest Third Rule, which requires:

  • Large quantity generators and small quantity generators to register for e-Manifest,
  • Exporters to submit manifests and continuation sheets to e-Manifest (and pay the associated fees), and
  • Waste handlers to submit manifest-related reports and data corrections to e-Manifest.

Streamlined recordkeeping for generators

Hazardous waste handlers using e-Manifest automatically meet the recordkeeping requirements to maintain records of manifests (paper or electronic) since the manifests are retained electronically in the system.

This eliminates the need to keep hard copies. It also provides a centralized place where handlers can access these documents at any time.

However, the provision doesn’t apply to generators using hybrid manifests; they must keep the initial paper copies of the electronic manifest for 3 years.

Reduced costs

Embracing electronic manifesting removes the costs associated with printing paper manifests from EPA-approved sources.

Keep in mind, there’s an unavoidable cost for receiving facilities and exporters. These entities have to pay user fees for each manifest they submit to e-Manifest.

Proactive preparation

EPA’s proposed Paper Manifest Sunset Rule would prohibit the use of paper manifests 2 years after the publication of a final rule. Hazardous waste handlers who transition to using only electronic manifests now will be better prepared to comply with future regulations. It gives businesses time to coordinate resources and address any unexpected issues.

Key to remember: Do you know the differences between hybrid and fully electronic hazardous waste manifests? The distinctions could be the difference between compliance and noncompliance.

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Most Recent Highlights In Safety & Health

EPA publishes first round of expiring TSCA CBI claims
2026-04-27T05:00:00Z

EPA publishes first round of expiring TSCA CBI claims

The Environmental Protection Agency (EPA) published the first list of expiring Confidential Business Information (CBI) claims for information submitted under the Toxic Substances Control Act (TSCA). The list covers CBI claims that expire from June 22, 2026, to July 31, 2026.

What are expiring CBI claims?

The Frank R. Lautenberg Chemical Safety for the 21st Century Act (which became law in June 2016) set an automatic 10-year expiration for most CBI claims made under TSCA. The first round of expiring claims starts in June 2026.

EPA allows businesses to request extensions of CBI protection for up to another 10 years.

How do I know if my CBI claims are expiring?

EPA will notify businesses of expiring CBI claims directly through the Central Data Exchange (CDX).

The agency will also release public lists of upcoming expiring CBI claims monthly on the “CBI Claim Expiration” webpage. The agency encourages businesses to review the lists to verify whether any of their claims are included.

How do I request an extension of expiring CBI claims?

Businesses seeking to extend a CBI claim beyond its expiration date must submit an extension request at least 30 days before the claim expires using the newly launched TSCA Section 14(e) CBI Claim Extension Request application in EPA’s CDX.

Here’s the general process:

  • EPA notifies the business of an expiring CBI claim directly through CDX and via the public lists on the “CBI Claim Expiration” webpage.
  • The business submits a request for extension through EPA’s CDX at least 30 days before the CBI claim expires. Requests must comply with the substantiation requirements at 40 CFR 703.5(a) and (b).
  • EPA reviews the submission and either grants or denies the request.

What are the possible results?

If EPA approves the extension request, the information in the CBI claim will remain protected for up to another 10 years.

If EPA denies the extension request, the agency can publicize the information in the claim 30 days after notifying the submitter in CDX. Further, if a business doesn’t submit an extension request at least 30 days before the expiration date, EPA may publicize the information without notifying the submitter.

Key to remember: EPA published the first round of expiring CBI claims for information submitted under TSCA. Businesses must submit extension requests to keep the information protected.

2026-04-24T05:00:00Z

North Dakota establishes AST regulations

Effective date: April 1, 2026

This applies to: Owners and operators of aboveground storage tanks (ASTs) and liquid fuel storage tanks

Description of change: The Department of Environmental Quality adopted technical standards and corrective action requirements for ASTs. The department also approved amendments to the registration dates and fee categories of the Petroleum Tank Release Compensation Fund for liquid fuels storage tanks.

Related state info: Aboveground storage tanks (ASTs) state comparison — ASTs

2026-04-24T05:00:00Z

Ohio finalizes sewage sludge amendments

Effective date: March 1, 2026

This applies to: Facilities regulated by the sewage sludge program

Description of change: The Ohio Environmental Protection Agency finalized changes to the sewage sludge program through its 5-year review of the regulations. The approved amendments:

  • Add professional operator of record requirements for privately owned treatment works;
  • Increase and add isolation distances for facilities;
  • Prohibit beneficial use of biosolids within a vulnerable hydrogeological setting;
  • Remove dioxin monitoring requirements; and
  • Add requirements for beneficial user certification (including the application and examination process, recordkeeping requirements, and reasons for suspending or revoking a certification).
2026-04-24T05:00:00Z

New Mexico adopts Clean Transportation Fuel Program rules

Effective date: April 1, 2026

This applies to: Transportation fuel produced in, imported into, or dispensed for use in New Mexico

Description of change: The New Mexico Environment Department finalized regulations to implement the Clean Transportation Fuel Program (CTFP) to reduce the carbon intensity of transportation fuel (including gasoline and diesel). The program covers transportation fuel producers, importers, and dispensers.

The CTFP:

  • Establishes annual statewide carbon intensity standards that apply to transportation fuel (e.g., gasoline and diesel) produced, imported, and dispensed for use in New Mexico;
  • Allocates credits and calculates deficits for regulated entities based on the fuel’s carbon intensity; and
  • Sets up a marketplace for selling and purchasing credits to comply with the carbon intensity standards.

The first compliance period runs from April 1, 2026, to December 31, 2027. The first compliance period report is due by April 30, 2028. Annual compliance reports will be due by April 30 for the previous calendar year.

2026-04-24T05:00:00Z

Maine lists materials covered for packaging stewardship program

Effective date: March 3, 2026

This applies to: Entities subject to the Stewardship Program for Packaging Regulations

Description of change: The Maine Department of Environmental Protection’s amendments to the Stewardship Program for Packaging Regulations (06-096 C.M.R. Chapter 428) include:

  • Aligning the rules with changes made by An Act to Improve Recycling by Updating the Stewardship Program for Packaging (L.D. 1423), and
  • Adding Appendix A — The Packaging Material Types List to the Stewardship Program for Packaging Regulations.

L.D. 1423:

  • Excludes certain commercial, cosmetic, medical, environmental, dangerous, hazardous, and flammable product packaging from the program requirements;
  • Excludes packaging of products related to public health and water quality testing from the program requirements;
  • Requires the department to adopt a process for approving a producer payment system; and
  • Updates definitions for clarity.

Appendix A defines packaging material and designates the material types readily recyclable as applicable. It may also designate materials as compostable or reusable.

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2026-04-24T05:00:00Z

California adopts permanent illegal disposal rules

Effective date: March 4, 2026

This applies to: Entities that handle, transfer, compost, transform, or dispose of solid waste

Description of change: CalRecycle made permanent the current illegal disposal emergency regulations, allowing enforcement agencies to take action against any person who illegally disposes of solid waste.

The rule also:

  • Adds the land application activities to the regulations, making the activities subject to the permitting tier structure and associated requirements (i.e., operator filing requirements, state minimum standards, recordkeeping, and enforcement agency inspection requirements); and
  • Amends sampling and recordkeeping for solid waste facilities, operations, and activities.
2026-04-24T05:00:00Z

West Virginia establishes fee schedule for UIC Program

Effective date: March 4, 2026

This applies to: Underground Injection Control (UIC) Program permittees

Description of change: This rule establishes the schedules of fees for carbon dioxide capture and sequestration authorized by the West Virginia Department of Environmental Protection’s (WVDEP’s) Division of Water and Waste Management.

EPA granted primacy to the WVDEP to implement the UIC Program for Class VI wells in February 2025.

2026-04-24T05:00:00Z

Colorado extends timeline to comply with GHG intensity targets

Effective date: April 14, 2026

This applies to: Small operators in the oil and gas sector

Description of change: The Colorado Air Quality Control Commission revised the intensity targets for reducing greenhouse gas (GHG) emissions for small oil and gas operators (those with less than 45 thousand barrels of oil equivalent (kBOE) production in 2025). The commission extended the first deadline to 2030 for small operators to meet applicable intensity requirements.

However, small operators must still submit the intensity plan for the 2027 targets, which is due by June 30, 2026.

Related state info: Clean air operating permits state comparison — Clean air operating permits

2026-04-24T05:00:00Z

Colorado finalizes state dredge and fill permit regulations

Effective date: March 30, 2026

This applies to: Projects that require preconstruction notification or compensatory mitigation

Description of change: The Colorado Water Quality Control Division finalized rules for implementing a state dredge and fill discharge authorization program established by HB24-1379. The program covers state waters that aren’t subject to federal dredge and fill permitting requirements under Section 404 of the Clean Water Act.

The division will continue issuing Temporary Authorizations until August 31, 2026. After that, applicants must apply for coverage under General Authorizations. The division already accepts applications for Individual Authorizations.

Related state info: Construction water permitting — Colorado

2026-04-24T05:00:00Z

New York adds wastewater cybersecurity rules

Effective date: March 26, 2026

This applies to: Wastewater treatment facilities

Description of change: The New York State Department of Environmental Conservation added cybersecurity regulations for wastewater treatment facilities. The rules:

  • Require all State Pollutant Discharge Elimination System (SPDES) permittees to report cybersecurity incidents,
  • Require publicly owned treatment works (POTWs) to establish, maintain, and implement an Emergency Response Plan and certify compliance with the provisions annually by March 28;
  • Establish baseline cybersecurity control requirements;
  • Add network monitoring and logging for certain POTWs with design flows of 10 million+ gallons per day; and
  • Require wastewater treatment plant operators to complete a minimum number of training hours within their existing required hours on cybersecurity to renew certification every 5 years.
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New Network Poll
Required General Industry OSHA Medical Surveillance Requirements At-A-Glance

Required General Industry OSHA Medical Surveillance Requirements At-A-Glance

Workers exposed to regulated substances in the workplace (e.g., lead, silica, asbestos) have an elevated risk for occupational diseases. OSHA requires employers to screen these workers for potential exposures with a focus on early detection of illness.

Medical surveillance is a systematic, complex process that looks for problems in the workplace identified by looking at abnormal screening results. Medical screening is one component of medical surveillance that assists with analyzing work group trends.

OSHA’s requirements rely on clinical reviews of an employee’s work history, medical history, physical assessment, and biological testing. Employers must provide medical examinations under the supervision of a licensed physician, without cost to employees, without loss of pay, and at a reasonable time and place. Records must be maintained in the strictest confidence to protect individual employee privacy.

This table summarizes OSHA’s general industry regulations that contain medical surveillance requirements; it does not cover EPA or other agency requirements.

*Have a Training Management Center Account already? Click the training links below to view our applicable training for the topic.

1910.95 Occupational noise exposure
Who:Employees whose occupational noise exposure equals or exceeds 85 decibels over an 8-hour time-weighted average (TWA).
Frequency:Audiograms.
  • Baseline audiogram must be given within 6 months of an employee’s exposure at or above the action level (85 decibels over an 8-hour time-weighted average (TWA)).
  • Annual audiogram must be offered thereafter.
Mobile test van exception. Where mobile test vans are used to meet the audiometric testing obligation, employers must obtain a valid baseline audiogram within 1 year of an employee’s first exposure at or above the action level.
Records:Audiometric test records. Must be kept for the duration of the affected employee’s employment, and include:
  • Name and job classification of employee,
  • Date of audiogram,
  • Examiner’s name,
  • Date of the last acoustic or exhaustive calibration of the audiometer, and
  • Employee’s most recent noise exposure assessment.

Noise exposure measurement records. Must be kept for 2 years.
Training link(s):
1910.120 Hazardous Waste Operations and Emergency Response (HAZWOPER)
Who:
  • All employees who are or may be exposed to hazardous substances or health hazards at or above the permissible exposure limits (PEL) or, if there is no PEL, above the published exposure levels for these substances, without regard to the use of respirators, for 30 days or more a year [1910.120(f)(2)(i)];
  • All employees who wear a respirator for 30 days or more a year or as required by 1910.134 [1910.120(f)(2)(ii)];
  • All employees who are injured, become ill, or develop signs or symptoms due to possible overexposure involving hazardous substances or health hazards from an emergency response or hazardous waste operation [1910.120(f)(2)(iii)]; and
  • Members of HAZMAT teams [1910.120(f)(2)(iv)].
Frequency:For employees covered under paragraphs (f)(2)(i), (f)(2)(ii), and (f)(2)(iv) [see above entry], medical examinations and consultations must be made available:
  • Prior to assignment;
  • At least once every 12 months for each employee covered unless the attending physician believes a longer interval (not greater than biennially) is appropriate;
  • As soon as possible upon notification by an employee that the employee has developed signs or symptoms indicating possible overexposure to hazardous substances or health hazards, or that the employee has been injured or exposed above the permissible exposure limits or published exposure levels in an emergency situation; and
  • At termination of employment or reassignment to an area where the employee would not be covered if the employee has not had an examination within the last 6 months;
  • At more frequent times, if the examining physician determines that an increased frequency of examination is medically necessary.

For employees covered under 1910.120(f)(2)(iii) [see above entry] and for all employees including those of employers covered by 1910.120(a)(1)(v) who may have been injured, received a health impairment, developed signs or symptoms which may have resulted from exposure to hazardous substances resulting from an emergency incident, or exposed during an emergency incident to hazardous substances at concentrations above the permissible exposure limits or the published exposure levels without the necessary personal protective equipment being used:
  • As soon as possible following the emergency incident or development of signs or symptoms, and
  • At additional times, if the examining physician determines that follow-up examinations or consultations are medically necessary.
Records:Medical surveillance records. Must be kept for at least the duration of employment plus 30 years, and include:
  • The name of the employee;
  • Physician’s written opinions, recommended limitations, and results of examinations and tests;
  • Any employee medical complaints related to exposure to hazardous substances;
  • A copy of the information provided to the examining physician by the employer, with the exception of the standard and its appendices.
Training link(s):
1910.134 Respiratory protection
Who:Employees required to use a respirator in the workplace.
Frequency:Medical evaluation. Must be provided before an employee is fit tested or required to use a respirator in the workplace, to determine employee’s ability to wear a respirator.

Additional medical evaluations. Must be provided if:
  • An employee reports medical signs or symptoms that are related to ability to use a respirator;
  • A physician or other licensed health care professional (PLHCP), supervisor, or the respirator program administrator informs the employer that an employee needs to be reevaluated;
  • Information from the respiratory protection program, including observations made during fit testing and program evaluation, indicates a need for employee reevaluation; or
  • A change occurs in workplace conditions (e.g., physical work effort, protective clothing, temperature) that may result in a substantial increase in the physiological burden placed on an employee.

Medical evaluations may be discontinued when the employee is no longer required to use a respirator.
Records:Medical evaluation records. Must be kept for at least the duration of employment plus 30 years.
Training link(s):
1910.1001 Asbestos
Who:Employees who are or will be exposed to airborne concentrations of fibers of asbestos at or above the time-weighted average (TWA) and/or excursion limit.

TWA. Airborne concentration of asbestos in excess of 0.1 fiber per cubic centimeter of air as an 8-hour TWA.

Excursion limit. Airborne concentration of asbestos in excess of 1.0 fiber per cubic centimeter of air (1 f/cc) as averaged over a sampling period of 30 minutes.
Frequency:Pre-placement examinations. Must be provided or made available before an employee is assigned to an occupation exposed to airborne concentrations of asbestos fibers at or above the TWA and/or excursion limit.

Periodic examinations. Must be made available annually.

Termination of employment examinations. Must be provided or made available and given within 30 calendar days before or after the date of termination of employment.

Recent examinations. No medical examination is required of any employee, if adequate records show that the employee has been examined in accordance with pre-placement, periodic, or termination examination requirements within the past 1-year period. A pre-employment medical examination which was required as a condition of employment by the employer, may not be used to meet the requirements of a recent examination, unless the cost of that examination is borne by the employer.
Records:Exposure measurements. Must be kept for at least 30 years and include:
  • The date of measurement;
  • The operation involving exposure to asbestos which is being monitored;
  • Sampling and analytical methods used and evidence of their accuracy;
  • Number, duration, and results of samples taken;
  • Type of respiratory protective devices worn, if any; and
  • Name and exposure of the employees whose exposure are represented.

Medical surveillance records. Must be kept for the duration of employment plus 30 years and include:
  • The name of the employee,
  • Physician’s written opinions,
  • Any employee medical complaints related to exposure to asbestos, and
  • A copy of the information provided to the physician.
Training link(s):
1910.1003 13 Carcinogens (1910.1003 through 1910.1016)
Who:Employees considered for assignment to enter regulated areas, and for authorized employees.

Regulated area. An area where entry and exit are restricted and controlled.

Authorized employees. Employees whose duties require them to be in the regulated area and who have been specifically assigned by the employer.
Frequency:Pre-assignment physical evaluation. Must be provided before an employee is assigned to enter a regulated area.

Periodic physical examination. Must be provided at least annually following the pre-assignment examination.
Records:Medical examination records. Must be complete and accurate and kept for the duration of the employee’s employment.
1910.1017 Vinyl chloride
Who:Each employee exposed, without regard to the use of respirators, to vinyl chloride in excess of the action level.

Action level. A concentration of vinyl chloride of 0.5 ppm averaged over an 8-hour work day.
Frequency:Medical examinations. Must be provided:
  • At the time of initial assignment or upon institution of medical surveillance,
  • At least annually thereafter,
  • To employees exposed to an emergency.
Records:Monitoring and measuring records. Must:
  • State the date of such monitoring and measuring and the concentrations determined and identify the instruments and methods used, and
  • Include any additional information necessary to determine individual employee exposures where such exposures are determined by means other than individual monitoring of employees.

Medical records. Must be kept for the duration of the employment of each employee plus 20 years, or 30 years, whichever is longer.

All records. Must include the name of each employee where relevant and be kept for not less than 30 years.
1910.1018 Inorganic arsenic
Who:
  • All employees who are or will be exposed above the action level, without regard to the use of respirators, at least 30 days per year; and
  • All employees who have been exposed above the action level, without regard to respirator use, for 30 days or more per year for a total of 10 years or more of combined employment with the employer or predecessor employers.

Action level. A concentration of inorganic arsenic of 5 micrograms per cubic meter of air (5 µg/m3) averaged over any 8-hour period.
Frequency:Initial examination. At the time of initial assignment to an area where the employee is likely to be exposed over the action level at least 30 days per year.

Periodic examination. Must be provided at least annually.

Termination examination. Whenever a covered employee has not taken a periodic examination within 6 months preceding the termination of employment, the employer must provide such examination to the employee upon termination of employment.

Additional examination. If the employee develops signs or symptoms commonly associated with exposure to inorganic arsenic the employer must provide an appropriate examination and emergency medical treatment.
Records:Exposure monitoring records. Must be kept for at least 40 years or for the duration of employment plus 20 years, whichever is longer, and include:
  • The date(s), number, duration location, and results of each of the samples taken, including a description of the sampling procedure used to determine representative employee exposure where applicable;
  • A description of the sampling and analytical methods used and evidence of their accuracy;
  • The type of respiratory protective devices worn, if any;
  • The environmental variables that could affect the measurement of the employee’s exposure.
  • Name and job classification of the employees monitored and of all other employees whose exposure the measurement is intended to represent; and

Medical surveillance records. Must be kept for at least 40 years or for the duration of employment plus 20 years, whichever is longer, and include:
  • The name and description of duties of the employee;
  • A copy of the physician’s written opinions;
  • Results of any exposure monitoring done for that employee and the representative exposure levels supplied to the physician; and
  • Any employee medical complaints related to exposure to inorganic arsenic.

Additional records. The employer must keep (or assure the examining physician keeps) the following medical records for at least 40 years, or for the duration of employment plus 20 years, whichever is longer:
  • A copy of the medical examination results including medical and work history;
  • A description of the laboratory procedures and a copy of any standards or guidelines used to interpret the test results or references to that information;
  • The initial X-ray;
  • Any X-rays with a demonstrated abnormality and all subsequent X-rays.
  • The X-rays for the most recent 5 years; and
1910.1024 Beryllium
Who:Employees who:
  • Are or are reasonably expected to be exposed at or above the action level for more than 30 days per year,
  • Show signs or symptoms of chronic beryllium disease (CBD) or other beryllium-related health effects,
  • Are exposed to beryllium during an emergency, or
  • Whose most recent written medical opinion required by 1910.1024(k)(6) or (k)(7) recommends periodic medical surveillance.

Action level. A concentration of airborne beryllium of 0.1 micrograms per cubic meter of air (μg/m3) calculated as an 8-hour time-weighted average (TWA).

Permissible Exposure Limits (PELs):

Time-weighted average (TWA) PEL. An airborne concentration of beryllium in excess of 0.2 μg/m3 calculated as an 8-hour TWA.

Short-term exposure limit (STEL). An airborne concentration of beryllium in excess of 2.0 μg/m3 as determined over a sampling period of 15 minutes.
Frequency:Medical examinations. Must be provided within 30 days and at least every 2 years thereafter.
Records:Air monitoring data. Employers must make and maintain a record of all exposure measurements taken to assess airborne exposure and maintain them for at least 30 years. The records must include at least:
  • The date of measurement for each sample taken;
  • The task that is being monitored;
  • The sampling and analytical methods used and evidence of their accuracy;
  • The number, duration, and results of samples taken;
  • The type of personal protective clothing and equipment, including respirators, worn by monitored employees at the time of monitoring; and
  • The name and job classification of each employee represented by the monitoring, indicating which employees were actually monitored.

Medical surveillance records. Must be kept for at least 30 years and include:
  • Name and job classification;
  • A copy of all licensed physicians’ written medical opinions for each employee; and
  • A copy of the information provided to the PLHCP.
1910.1025 Lead
Who:Employees who are or may be exposed at or above the action level for more than 30 days per year.

Action level. Employee exposure, without regard to the use of respirators, to an airborne concentration of lead of 30 micrograms per cubic meter of air (30 µg/m3) averaged over an 8-hour period.
Frequency:Biological monitoring. Blood lead and zinc protoporphyrin (ZPP) level sampling and analysis must be made available:
  • At least every 6 months to each covered employee.
  • At least monthly during the removal period of each employee removed from exposure to lead due to an elevated blood lead level.
  • At least every 2 months for each employee whose last blood sampling and analysis indicated a blood lead level at or above 40 µg/100 g of whole blood. This frequency must continue until two consecutive blood samples and analyses indicate a blood lead level below 40 µg/100 g of whole blood; and

Follow-up blood sampling tests. Whenever the results of a blood lead level test indicate that an employee’s blood lead level is at or above the numerical criterion for medical removal under paragraph (k)(1)(i)(A) of 1910.1025, the employer must provide a second (follow-up) blood sampling test within 2 weeks after the employer receives the results of the first blood sampling test.

Medical examinations and consultations. Must be made available:
  • At least annually for each employee for whom a blood sampling test conducted at any time during the preceding 12 months indicated a blood lead level at or above 40 µg/100 g;
  • Prior to assignment for each employee being assigned for the first time to an area in which airborne concentrations of lead are at or above the action level;
  • As soon as possible, upon notification by an employee either that the employee has developed signs or symptoms commonly associated with lead intoxication, that the employee desires medical advice concerning the effects of current or past exposure to lead on the employee’s ability to procreate a healthy child, or that the employee has demonstrated difficulty in breathing during a respirator fitting test or during use; and
  • As medically appropriate for each employee either removed from exposure to lead due to a risk of sustaining material impairment to health, or otherwise limited pursuant to a final medical determination.
Records:Exposure monitoring records. Must be kept for at least 40 years or for the duration of employment plus 20 years, whichever is longer, and include:
  • The date(s), number, duration, location and results of each of the samples taken, including a description of the sampling procedure used to determine representative employee exposure where applicable;
  • A description of the sampling and analytical methods used and evidence of their accuracy;
  • The type of respiratory protective devices worn, if any;
  • The environmental variables that could affect the measurement of employee exposure.
  • Name and job classification of the employee monitored and of all other employees whose exposure the measurement is intended to represent; and

Medical surveillance. Must be kept for the duration of employment plus 30 years and include:
  • The name and description of the duties of the employee;
  • A copy of the physician’s written opinions;
  • Results of any airborne exposure monitoring done for that employee and the representative exposure levels supplied to the physician; and
  • Any employee medical complaints related to exposure to lead.

Medical records. Must be kept by the employer or the examining physician for at least 40 years, or for the duration of employment plus 20 years, whichever is longer, and include:
  • A copy of the medical examination results including medical and work history,
  • A description of the laboratory procedures and a copy of any standards or guidelines used to interpret the test results or references to that information, and
  • A copy of the results of biological monitoring.

Medical removal records for employees removed from current exposure to lead. Must be kept for at least the duration of an employee’s employment and include:
  • The name of the employee,
  • The date on each occasion that the employee was removed from current exposure to lead as well as the corresponding date on which the employee was returned to his or her former job status,
  • A brief explanation of how each removal was or is being accomplished, and
  • A statement with respect to each removal indicating whether or not the reason for the removal was an elevated blood lead level.
Training link(s):
1910.1026 Chromium (VI)
Who:Employees who:
  • Are or may be occupationally exposed to chromium (VI) ‒ commonly referred to as hexavalent chromium ‒ at or above the action level for 30 or more days a year,
  • Experience signs or symptoms of the adverse health effects associated with chromium (VI) exposure, or
  • Are exposed in an emergency.

Action level. A concentration of airborne chromium (VI) of 2.5 micrograms per cubic meter of air (2.5 µgm/m3) calculated as an 8-hour time-weighted average (TWA).

Permissible exposure limit (PEL). An airborne concentration of chromium (VI) in excess of 5 micrograms per cubic meter of air (5 µgm/m3), calculated as an 8-hour time-weighted average (TWA).
Frequency:Medical examinations. Must be provided:
  • Within 30 days after initial assignment, unless the employee has received a chromium (VI) related medical examination that meets the requirements of 1910.1026(k) within the last 12 months;
  • Annually;
  • Within 30 days after a physician or other license healthcare professional’s (PLHCP) written medical opinion recommends an additional examination;
  • Whenever an employee shows signs or symptoms of the adverse health effects associated with chromium (VI) exposure;
  • Within 30 days after exposure during an emergency which results in an uncontrolled release of chromium (VI); or
  • At the termination of employment, unless the last examination that satisfied the requirements of 1910.1026(k) was less than 6 months prior to the date of termination.
Records:Air monitoring data. Must be kept for at least 30 years and include:
  • The date of measurement for each sample taken;
  • The operation involving exposure to chromium (VI) that is being monitored;
  • Sampling and analytical methods used and evidence of their accuracy;
  • Number, duration, and the results of samples taken;
  • Type of personal protective equipment, such as respirators worn; and
  • Name and job classification of all employees represented by the monitoring, indicating which employees were actually monitored.

Historical monitoring data. Where the employer has relied on historical monitoring data to determine exposure to chromium (VI), these records must be kept for at least 30 years and include:
  • The data were collected using methods that meet the accuracy requirements of 1910.1026(d)(5);
  • The processes and work practices that were in use when the historical monitoring data were obtained are essentially the same as those to be used during the job for which exposure is being determined;
  • The characteristics of the chromium (VI) containing material being handled when the historical monitoring data were obtained are the same as those on the job for which exposure is being determined;
  • Environmental conditions prevailing when the historical monitoring data were obtained are the same as those on the job for which exposure is being determined; and
  • Other data relevant to the operations, materials, processing, or employee exposures covered by the exception.

Objective data. An accurate record of all objective data relied upon to comply with the requirements of 1910.1026 must be kept for 30 years and include:
  • The chromium containing material in question;
  • The source of the objective data;
  • The testing protocol and results of testing, or analysis of the material for the release of chromium (VI);
  • A description of the process, operation, or activity and how the data support the determination; and
  • Other data relevant to the process, operation, activity, material, or employee exposures.

Medical surveillance records. Must be kept for 30 years and include:
  • Name;
  • A copy of the PLHCP’s written opinions; and
  • A copy of the information provided to the PLHCP.
1910.1027 Cadmium
Who:
  • Employees who are or may be exposed to cadmium at or above the action level unless the employer demonstrates that the employee is not, and will not be, exposed at or above the action level on 30 or more days per year (12 consecutive months); and
  • Employees who prior to the effective date of 1910.1027 (Sept. 14, 1992) might previously have been exposed to cadmium at or above the action level by the employer, unless the employer demonstrates that the employee did not prior to Sept. 14, 1992, work for the employer in jobs with exposure to cadmium for an aggregated total of more than 60 months.

Action level. An airborne concentration of cadmium of 2.5 micrograms per cubic meter of air (2.5 µg/m3), calculated as an 8-hour time-weighted average (TWA).
Frequency:Initial (preplacement) examinations. Must be provided within 30 days after initial assignment to a job with exposure to cadmium.

Recent examinations. An initial examination is not required to be provided if adequate records show that the employee was examined in accordance with the requirements of paragraph (l)(2)(ii) of 1910.1027 within the past 12 months. In that case, such records must be maintained as part of the employee’s medical record and the prior exam must be treated as if it were an initial examination for the purposes of paragraphs (l)(3) and (4) of 1910.1027.

Periodic medical surveillance. Must be provided within 1 year after the initial examination and thereafter at least biennially. Biological sampling must be provided at least annually, either as part of a periodic medical examination or separately as periodic biological monitoring.

Examination for respirator use. Must be provided prior to the employee’s being assigned to a job that requires the use of a respirator, to any employee without a medical examination within the preceding 12 months that satisfies the requirements of 1910.1027(l)(6)(i).

Emergency examinations. Must be provided as soon as possible to any employee who may have been acutely exposed to cadmium because of an emergency.

Termination of employment examinations. At termination of employment, the employer must provide a medical examination in accordance with paragraph (l)(4)(ii) of 1910.1027, to any employee to whom at any prior time the employer was required to provide medical surveillance. If the last examination satisfied the requirements of paragraph (l)(4)(ii) and was less than 6 months prior to the date of termination, no further examination is required unless otherwise specified in paragraphs (l)(3) or (l)(5).

If the employer has discontinued all periodic medical surveillance under paragraph 1910.1027(l)(4)(v), no termination of employment medical examination is required.
Records:Medical surveillance records. Must be kept for the duration of employment plus 30 years, and include:
  • Name and description of the duties;
  • A copy of the physician’s written opinions and an explanation sheet for biological monitoring results;
  • A copy of the medical history, and the results of any physical examination and all test results that are required to be provided by 1910.1027, including biological tests, X-rays, pulmonary function tests, etc., or that have been obtained to further evaluate any condition that might be related to cadmium exposure;
  • The employee’s medical symptoms that might be related to exposure to cadmium; and
  • A copy of the information provided to the physician.
Training link(s):
1910.1028 Benzene
Who:Employees who:
  • Are or may be exposed to benzene at or above the action level 30 or more days per year;
  • Are or may be exposed to benzene at or above the permissible exposure limits (PELs) 10 or more days per year;
  • Have been exposed to more than 10 ppm of benzene for 30 or more days in a year prior to the effective date of the standard when employed by their current employer; and
  • Are involved in the tire building operations called tire building machine operators, who use solvents containing greater than 0.1 percent benzene.

Action level. An airborne concentration of benzene of 0.5 ppm calculated as an 8-hour time-weighted average (TWA).

PELs:

Time-weighted average limit (TWA). An airborne concentration of benzene in excess of one part of benzene per million parts of air (1 ppm) as an 8-hour TWA.

Short-term exposure limit (STEL). An airborne concentration of benzene in excess of 5 ppm as averaged over any 15-minute period.
Frequency:Initial examinations. Before the time of initial assignment.

Periodic examinations. At least annually following the initial examination.

Emergency examinations. If an employee is exposed to benzene in an emergency situation, the employer must have the employee provide a urine sample at the end of the employee’s shift and have a urinary phenol test performed on the sample within 72 hours.
Records:Exposure measurements. Must be kept for at least 30 years and include:
  • The dates, number, duration, and results of each of the samples taken, including a description of the procedure used to determine representative employee exposures;
  • A description of the sampling and analytical methods used;
  • A description of the type of respiratory protective devices worn, if any; and
  • The name, job classification, and exposure levels of the employee monitored and all other employees whose exposure the measurement is intended to represent.

Medical surveillance records. Must be kept for the duration of employment plus 30 years, and include:
  • The name of the employee;
  • The employer’s copy of the physician’s written opinion on the initial, periodic and special examinations, including results of medical examinations and all tests, opinions and recommendations;
  • Any employee medical complaints related to exposure to benzene;
  • A copy of the information provided to the physician; and
  • A copy of the employee’s medical and work history related to exposure to benzene or any other hematologic toxins.
Training link(s):
1910.1029 Coke oven emissions
Who:Employees who are employed in a regulated area at least 30 days per year.

Regulated area. An area defined at 1910.1029(d) with access limited to authorized persons.

Permissible exposure limit. Employees in the regulated area must not be exposed to coke oven emissions at concentrations greater than 150 micrograms per cubic meter of air (150 µg/m3), averaged over any 8-hour period.
Frequency:Initial examinations. Must be provided at the time of initial assignment to a regulated area or upon the institution of the medical surveillance program.

Periodic examinations. Must be provided at least annually.
Records:Medical surveillance records. Must include:
  • Name and description of duties of the employee,
  • A copy of the physician’s written opinion,
  • The signed statement of any refusal to take a medical examination, and
  • Any employee medical complaints related to exposure to coke oven emissions.

Medical records. The employer must keep, or assure that the examining physician keeps:
  • A copy of the medical examination results including medical and work history,
  • The initial x-ray,
  • A description of the laboratory procedures used and a copy of any standards or guidelines used to interpret the test results,
  • The x-rays for the most recent 5 years,
  • Any x-ray with a demonstrated abnormality and all subsequent x-rays,
  • The initial cytologic examination slide and written description,
  • The cytologic examination slide and written description for the most recent 10 years, and
  • Any cytologic examination slides with demonstrated atypia, if such atypia persists for 3 years, and all subsequent slides and written descriptions.

All medical records and medical surveillance records. Must be kept for at least 40 years, or for the duration of employment plus 20 years, whichever is longer.
Training link(s):
1910.1030 Bloodborne pathogens
Who:Employees with occupational exposure to bloodborne pathogens, as defined at 1910.1030(b).
Frequency:Hepatitis B vaccine and vaccination series. Must be offered to all employees with occupational exposure.

Post-exposure evaluation and follow-up. Must be made immediately available to all employees who have had an exposure incident.
Records:Medical records. Must be kept for the duration of employment plus 30 years and include:
  • The name of the employee;
  • A copy of the employee’s hepatitis B vaccination status including the dates of all the hepatitis B vaccinations and any medical records relative to the employee’s ability to receive vaccination;
  • The employer’s copy of the healthcare professional’s written opinion; and
  • A copy of all results of examinations, medical testing, and follow-up procedures;
  • A copy of the information provided to the healthcare professional.
Training link(s):
1910.1043 Cotton dust
Who:Employees exposed to cotton dust.

Action levels:

Yarn manufacturing and cotton washing operations: Airborne concentration of lint-free respirable cotton dust of 100 µg/m3 mean concentration, averaged over an 8-hour period, as measured by a vertical elutriator or an equivalent instrument.

Waste houses for textile operations: Airborne concentration of lint-free respirable cotton dust of 250 µg/m3 mean concentration, averaged over an 8-hour period, as measured by a vertical elutriator or an equivalent instrument.

Textile processes known as slashing and weaving: Airborne concentration of lint-free respirable cotton dust of 375 µg/m3 mean concentration, averaged over an 8-hour period, as measured by a vertical elutriator or an equivalent instrument.
Frequency:Initial examinations. Must be provided to each employee who is or may be exposed to cotton dust. New employees must be provided an examination prior to initial assignment.

Periodic examinations. Must be provided:
  • At least annually for all employees exposed to cotton dust above the action level in yarn manufacturing, slashing and weaving, cotton washing and waste house operations
  • At least every 2 years for all employees exposed to cotton dust at or below the action level, for all employees exposed to cotton dust from washed cotton (except from washed cotton defined in 1910.1043(n)(3)), and for all employees exposed to cotton dust in cottonseed processing and waste processing operations.
Records:Medical records. Must be kept for at least 20 years and include:
  • The name and description of the duties of the employee;
  • A copy of the medical examination results including the medical history, questionnaire response, results of all tests, and the physician’s recommendation;
  • A copy of the physician’s written opinion;
  • Any employee medical complaints related to exposure to cotton dust;
  • A copy of 1910.1043 and its appendices, except that employers may keep one copy of the standard and the appendices for all employees, provided that they reference 1910.1043 and appendices in the medical surveillance record of each employee; and
  • A copy of the information provided to the physician.
Training link(s):
1910.1044 – 1,2-dibromo-3-chloropropane
Who:Employees who work in regulated areas and those who are subjected to DBCP exposures in an emergency situation. Regulated areas are those where DBCP concentrations are in excess of the permissible exposure limit (PEL).

PEL:

Inhalation. Airborne concentration of DBCP in excess of 1 part DBCP per billion parts of air (ppb) as an 8-hour time-weighted average (TWA).

Dermal and eye exposure. No employee must be exposed to skin or eye contact with DBCP.
Frequency:Medical examinations. Must be provided at the time of initial assignment and annually thereafter.
Records:Medical records. Must be kept for at least 40 years or the duration of employment plus 20 years, whichever is longer, and include:
  • The name of the employee,
  • A copy of the physician’s written opinion,
  • Any employee medical complaints related to exposure to DBCP,
  • A copy of the information provided the physician, and
  • A copy of the employee’s medical and work history.
1910.1045 Acrylonitrile
Who:Employees who are or will be exposed to AN at or above the action level, without regard to the use of respirators.

Action level. A concentration of AN of 1 ppm as an 8-hour time-weighted average (TWA).
Frequency:Initial examinations. Must be provided at the time of initial assignment or upon institution of the medical surveillance program.

Periodic examinations. Must be provided at least annually. If an employee has not had the initial examination within 6 months preceding termination of employment, the employer must make such examination available to the employee prior to termination.

Additional examinations. Must be provided to employees who develop signs or symptoms which may be associated with exposure to AN.
Records:Medical records. Must be kept for at least 40 years, or for the duration of employment plus 20 years, whichever is longer, and include:
  • A copy of the physician’s written opinions,
  • Any employee medical complaints related to exposure to AN,
  • A copy of the information provided to the physician, and
  • A copy of the employee’s medical and work history.
Training link(s):
1910.1047 Ethylene oxide
Who:All employees who are or may be exposed to EtO at or above the action level, without regard to the use of respirators, for at least 30 days a year, and all employees who have been exposed to EtO in an emergency situation.

Action level. A concentration of airborne EtO of 0.5 ppm calculated as an 8-hour time-weighted average (TWA).
Frequency:Medical examinations. Must be provided:
  • Prior to assignment of the employee to an area where exposure may be at or above the action level for at least 30 days a year.
  • At least annually for each employee exposed at or above the action level for at least 30 days in the past year.
  • At termination of employment or reassignment to an area where exposure to EtO is not at or above the action level for at least 30 days a year.
  • As medically appropriate for any employee exposed during an emergency.
  • As soon as possible, upon notification by an employee either (1) that the employee has developed signs or symptoms indicating possible overexposure to EtO, or (2) that the employee desires medical advice concerning the effects of current or past exposure to EtO on the employee’s ability to produce a healthy child.
  • If the examining physician determines that any of the examinations should be provided more frequently than specified, the employer must provide such examinations to affected employees at the frequencies recommended by the physician.
Records:Medical records. Must be kept for the duration of employment plus 30 years and include:
  • The name of the employee,
  • Physicians’ written opinions,
  • Any employee medical complaints related to exposure to EtO, and
  • A copy of the information provided to the physician.
1910.1048 Formaldehyde
Who:
  • Employees who are exposed to formaldehyde at concentrations at or exceeding the action level or exceeding the short-term exposure limit (STEL), or in emergencies.
  • Employees who develop signs and symptoms of overexposure to formaldehyde.

Action level. A concentration of 0.5 part formaldehyde per million parts of air (0.5 ppm) calculated as an 8-hour time-weighted average (TWA) concentration.

Short-term exposure limit (STEL). An airborne concentration of formaldehyde which exceeds two parts formaldehyde per million parts of air (2 ppm) as a 15-minute STEL.
Frequency:Medical examinations. Must be given:
  • To any employee who the physician feels, based on information in the medical disease questionnaire, may be at increased risk from exposure to formaldehyde.
  • At the time of initial assignment.
  • At least annually thereafter to all employees required to wear a respirator to reduce exposure to formaldehyde.

Emergency medical examinations. Must be made available as soon as possible to all employees who have been exposed to formaldehyde in an emergency.
Records:Medical records. Must be kept for the duration of employment plus 30 years and include:
  • The name of the employee;
  • The physician’s written opinion;
  • A list of any employee health complaints that may be related to exposure to formaldehyde; and
  • A copy of the medical examination results, including medical disease questionnaires and results of any medical tests required by the standard or mandated by the examining physician.
1910.1050 Methylenedianiline
Who:
  • Employees exposed to MDA at or above the action level for 30 or more days per year;
  • Employees subject to dermal exposure to MDA for 15 or more days per year;
  • Employees exposed in an emergency situation;
  • Employees whom the employer, based on results from compliance with paragraph 1910.1050(e)(8), has reason to believe are being dermally exposed; and
  • Employees who show signs or symptoms of MDA exposure.

Action level. A concentration of airborne MDA of 5 ppb as an 8-hour time-weighted average (TWA).

Dermal exposure to MDA. Occurs where employees are engaged in the handling, application, or use of mixtures or materials containing MDA, with any of the following non-airborne forms of MDA:
  • Liquid, powdered, granular, or flaked mixtures containing MDA in concentrations greater than 0.1% by weight or volume; and
  • Materials other than “finished articles” containing MDA in concentrations greater than 0.1% by weight or volume.
Frequency:Initial examinations. Before the time of initial assignment.

Periodic examinations. At least annually following the initial examination.

Emergency examinations. If the employer determines that the employee has been exposed to a potentially hazardous amount of MDA in an emergency situation.

Additional examinations. Where the employee develops signs and symptoms associated with exposure to MDA.
Records:Medical surveillance records. Must be kept for at least the duration of employment plus 30 years and include:
  • The name and description of the duties of the employee;
  • The employer’s copy of the physician’s written opinion on the initial, periodic, and any special examinations, including results of medical examination and all tests, opinions, and recommendations;
  • Results of any airborne exposure monitoring done for that employee and the representative exposure levels supplied to the physician; and
  • Any employee medical complaints related to exposure to MDA.

Medical records. The employer must keep, or assure that the examining physician keeps, for at least the duration of employment plus 30 years, the following medical records:
  • A copy of 1910.1050 and its appendices, except that the employer may keep one copy of the standard and its appendices for all employees provided the employer references the standard and its appendices in the medical surveillance record of each employee;
  • A copy of the information provided to the physician as required by any paragraphs in the regulatory text;
  • A description of the laboratory procedures and a copy of any standards or guidelines used to interpret the test results or references to the information; and
  • A copy of the employee’s medical and work history related to exposure to MDA.

Medical removal records. Records for employees removed from current exposure to MDA must be kept for at least the duration of an employee’s employment plus 30 years, and include:
  • The name of the employee,
  • The date of each occasion that the employee was removed from current exposure to MDA as well as the corresponding date on which the employee was returned to his or her former job status,
  • A brief explanation of how each removal was or is being accomplished, and
  • A statement with respect to each removal indicating the reason for the removal.
Training link(s):
1910.1051 1,3-Butadiene
Who
  • Employees with exposure to BD at concentrations at or above the action level on 30 or more days or for employees who have or may have exposure to BD at or above the permissible exposure limits (PELs) on 10 or more days a year.
  • Employers (including successor owners) must continue to provide medical screening and surveillance for employees, even after transfer to a non-BD exposed job and regardless of when the employee is transferred, whose work histories suggest exposure to BD:
    • At or above the PELs on 30 or more days a year for 10 or more years;
    • At or above the action level on 60 or more days a year for 10 or more years; or
    • Above 10 ppm on 30 or more days in any past year; and
    • Each employee exposed to BD following an emergency situation.

Action level. A concentration of airborne BD of 0.5 ppm calculated as an 8-hour time-weighted average (TWA).

Permissible exposure limits (PELs):

Time-weighted average (TWA) limit. No employee must be exposed to an airborne concentration of BD in excess of 1 part BD per million parts of air (ppm) measured as an 8-hour time-weighted average.

Short-term exposure limit (STEL). No employee must be exposed to an airborne concentration of BD in excess of 5 parts of BD per million parts of air (5 ppm) as determined over a sampling period of 15 minutes.
Frequency:Health questionnaire and complete blood count with differential and platelet count (CBC). Annually.

Initial physical examination. Must be given:
  • If 12 months or more have elapsed since the last physical examination conducted as part of a medical screening program for BD exposure,
  • Before assumption of duties by the employee in a job with BD exposure,
  • Every 3 years after the initial physical examination,
  • At the discretion of the physician or other licensed care professional reviewing the annual health questionnaire and CBD,
  • At termination of employment if 12 months or more have elapsed since the last physical examination.

Emergency medical screening. Must be conducted as quickly as possible but not later than 48 hours after the exposure.

Respirator fit test. For each employee who must wear a respirator, physical ability to perform the work and use the respirator must be determined as required by 1910.134.
Records:Exposure measurements. Records must be kept for at least 30 years and include:
  • The date of measurement;
  • The operation involving exposure to BD which is being monitored;
  • Sampling and analytical methods used and evidence of their accuracy;
  • Number, duration, and results of samples taken;
  • Type of protective devices worn, if any; and
  • Name and exposure of the employees whose exposures are represented.
  • The written corrective action and the schedule for completion of this action required by 1910.1051(d)(7)(ii).

Medical screening and surveillance records. Must kept for the duration of employment plus 30 years and include:
  • The name of the employee;
  • Physician’s or other licensed healthcare professional’s written opinions as described in 1910.1051(k)(7);
  • A copy of the information provided to the physician or other licensed healthcare professional as required by 1910.1051(k)(7)(ii)-(iv).
Training link(s):
1910.1052 Methylene chloride
Who:Employees who are or may be exposed to MC:
  • At or above the action level on 30 or more days per year, or above the 8-hour TWA permissible exposure limit (PEL) or the short-term exposure limit (STEL) on 10 or more days per year;
  • Above the 8-TWA PEL or STEL for any time period where an employee has been identified by a physician or other licensed health care professional as being at risk from cardiac disease or from some other serious MC-related health condition and such employee requests inclusion in the medical surveillance program; and
  • During an emergency.

Action level. A concentration of airborne MC of 12.5 parts per million (ppm) calculated as an 8-hour time-weighted average (TWA).

Eight-hour time-weighted average (TWA) PEL. Airborne concentration of MC in excess of 25 parts of MC per million parts of air (25 ppm) as an 8-hour TWA.

Short-term exposure limit (STEL). An airborne concentration of MC in excess of 125 parts of MC per million parts of air (125 ppm) as determined over a sampling period of 15 minutes.
Frequency:Medical evaluation. Before having an employee use a supplied-air respirator in the negative-pressure mode, or a gas mask with an organic-vapor canister for emergency escape, the employer must:
  • Have a physician or other licensed healthcare professional (PLHCP) evaluate the employee’s ability to use such respiratory protection.
  • Ensure that the PLHCP provides their findings in a written opinion to the employee and the employer.

Medical surveillance. Must be made available:
  • Initially, before the time of an employee’s initial assignment;
  • Annually thereafter;
  • When recommended in the written medical opinion; and
  • When an employee leaves the employer’s workplace or is reassigned to an area where exposure to MC is consistently at or below the action level and STEL, medical surveillance must be made available if 6 months or more have elapsed since the last medical surveillance.
Records:Medical surveillance records. Must be kept for the duration of employment plus 30 years, and include:
  • The name and description of the duties of the employee,
  • Written medical opinions, and
  • Any employee medical conditions related to exposure to MC.
1910.1053 Respirable crystalline silica
Who:Employees who will be occupationally exposed to respirable crystalline silica at or above the action level for 30 or more days per year.

Action level. A concentration of airborne respirable crystalline silica of 25 μg/m3, calculated as an 8-hour time-weighted average (TWA).
Frequency:Initial examinations. An initial (baseline) examination must be made available within 30 days after initial assignment, unless the employee has received a medical examination that meets the requirements of 1910.1053 within the last 3 years.

Periodic examinations. At least every 3 years, or more frequently if recommended by the physician or other licensed healthcare professional (PLHCP).

Additional examinations. If the PLHCP’s written medical opinion indicates that an employee should be examined by a specialist, the employer must make available a medical examination by a specialist within 30 days after receiving the PLHCP’s written opinion.
Records:Medical surveillance records. Must be kept for the duration of employment plus 30 years, and include:
  • Employee name,
  • A copy of the PLHCPs’ and specialists’ written medical opinions, and
  • A copy of the information provided to the PLHCPs and specialists.
Training link(s):
1910.1450 Occupational exposure to hazardous chemicals in laboratories
Who:Employees exposed above the action level or the permissible exposure limit (PEL) for an OSHA-regulated substance for which there are exposure monitoring and medical surveillance requirements.
Frequency:Medical examinations. Whenever employees develop signs or symptoms associated with a hazardous chemical to which they may have been exposed in the laboratory, they must be provided an opportunity to receive an appropriate medical examination.

Medical surveillance. Where exposure monitoring reveals an exposure level routinely above the action level (or in the absence of an action level, the permissible exposure limit (PEL)) for an OSHA-regulated substance for which there are exposure monitoring and medical surveillance requirements, medical surveillance must be established for the affected employee as prescribed by the particular standard.

Medical consultations. Whenever an event takes place in the work area such as a spill, leak, explosion, or other occurrence resulting in the likelihood of a hazardous exposure, the affected employee must be provided an opportunity for a medical consultation. The consultation must be for the purpose of determining the need for a medical examination.
Records:Medical and monitoring records. The following records must be kept for at least the duration of employment plus 30 years:
  • Any measurements taken to monitor employee exposures,
  • Any medical consultation, and
  • Examinations including tests or written opinions required by 1910.1450.
Training link(s):
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