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FMCSA updates the Medical Advisory Criteria published as an appendix in the Code of Federal Regulations (CFR). The appendix provides guidance for medical examiners listed on FMCSA's National Registry of Certified Medical Examiners (National Registry) on the applicability and interpretation of the physical qualification standards for operators of commercial motor vehicles. The advisory criteria in the appendix are also intended to provide recommendations and information to assist medical examiners in applying the standards, basic information related to testing, and matters to consider when making a qualification determination. The updated Medical Advisory Criteria replace all previous versions of the criteria.

DATES: This final rule is effective on January 19, 2024, published in the Federal Register January 19, 2024, page 3577.

View final rule.

Appendix A to Part 391—Medical Advisory Criteria
Entire appendixRevisedView text

Previous Text

Appendix A to Part 391—Medical Advisory Criteria

I. Introduction

This appendix contains the Agency’s guidelines in the form of Medical Advisory Criteria to help medical examiners assess a driver’s physical qualification. These guidelines are strictly advisory and were established after consultation with physicians, States, and industry representatives, and, in some areas, after consideration of recommendations from the Federal Motor Carrier Safety Administration’s Medical Review Board and Medical Expert Panels.

II. Interpretation of Medical Standards

Since the issuance of the regulations for physical qualifications of commercial motor vehicle drivers, the Federal Motor Carrier Safety Administration has published recommendations called Advisory Criteria to help medical examiners in determining whether a driver meets the physical qualifications for commercial driving. These recommendations have been condensed to provide information to medical examiners that is directly relevant to the physical examination and is not already included in the Medical Examination Report Form.

A. Loss of Limb: §391.41(b)(1)

A person is physically qualified to drive a commercial motor vehicle if that person: Has no loss of a foot, leg, hand or an arm, or has been granted a Skills Performance Evaluation certificate pursuant to §391.49.

B. Limb Impairment: §391.41(b)(2)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no impairment of:

(i) A hand or finger which interferes with prehension or power grasping; or

(ii) An arm, foot, or leg which interferes with the ability to perform normal tasks associated with operating a commercial motor vehicle; or

(iii) Any other significant limb defect or limitation which interferes with the ability to perform normal tasks associated with operating a commercial motor vehicle; or

(iv) Has been granted a Skills Performance Evaluation certificate pursuant to §391.49.

2. A person who suffers loss of a foot, leg, hand or arm or whose limb impairment in any way interferes with the safe performance of normal tasks associated with operating a commercial motor vehicle is subject to the Skills Performance Evaluation Certificate Program pursuant to §391.49, assuming the person is otherwise qualified.

3. With the advancement of technology, medical aids and equipment modifications have been developed to compensate for certain disabilities. The Skills Performance Evaluation Certificate Program (formerly the Limb Waiver Program) was designed to allow persons with the loss of a foot or limb or with functional impairment to qualify under the Federal Motor Carrier Safety Regulations by use of prosthetic devices or equipment modifications which enable them to safely operate a commercial motor vehicle. Since there are no medical aids equivalent to the original body or limb, certain risks are still present, and thus restrictions may be included on individual Skills Performance Evaluation certificates when a State Director for the Federal Motor Carrier Safety Administration determines they are necessary to be consistent with safety and public interest.

4. If the driver is found otherwise medically qualified (§391.41(b)(3) through (13)), the medical examiner must check on the Medical Examiner’s Certificate that the driver is qualified only if accompanied by a Skills Performance Evaluation certificate. The driver and the employing motor carrier are subject to appropriate penalty if the driver operates a motor vehicle in interstate or foreign commerce without a current Skill Performance Evaluation certificate for his/her physical disability.

C. [Reserved]

D. Cardiovascular Condition: §391.41(b)(4)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no current clinical diagnosis of myocardial infarction, angina pectoris, coronary insufficiency, thrombosis or any other cardiovascular disease of a variety known to be accompanied by syncope, dyspnea, collapse or congestive cardiac failure.

2. The term “has no current clinical diagnosis of” is specifically designed to encompass: “a clinical diagnosis of” a current cardiovascular condition, or a cardiovascular condition which has not fully stabilized regardless of the time limit. The term “known to be accompanied by” is designed to include a clinical diagnosis of a cardiovascular disease which is accompanied by symptoms of syncope, dyspnea, collapse or congestive cardiac failure; and/or which is s likely to cause syncope, dyspnea, collapse or congestive cardiac failure.

3. It is the intent of the Federal Motor Carrier Safety Regulations to render unqualified, a driver who has a current cardiovascular disease which is accompanied by and/or likely to cause symptoms of syncope, dyspnea, collapse, or congestive cardiac failure. However, the subjective decision of whether the nature and severity of an individual’s condition will likely cause symptoms of cardiovascular insufficiency is on an individual basis and qualification rests with the medical examiner and the motor carrier. In those cases where there is an occurrence of cardiovascular insufficiency (myocardial infarction, thrombosis, etc.), it is suggested before a driver is certified that he or she have a normal resting and stress electrocardiogram, no residual complications and no physical limitations, and is taking no medication likely to interfere with safe driving.

4. Coronary artery bypass surgery and pacemaker implantation are remedial procedures and thus, not medically disqualifying. Implantable cardioverter defibrillators are disqualifying due to risk of syncope. Coumadin is a medical treatment which can improve the health and safety of the driver and should not, by its use, medically disqualify the commercial motor vehicle driver. The emphasis should be on the underlying medical condition(s) which require treatment and the general health of the driver. The Federal Motor Carrier Safety Administration should be contacted at (202) 366-4001 for additional recommendations regarding the physical qualification of drivers on coumadin.

E. Respiratory Dysfunction: §391.41(b)(5)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no established medical history or clinical diagnosis of a respiratory dysfunction likely to interfere with ability to control and drive a commercial motor vehicle safely.

2. Since a driver must be alert at all times, any change in his or her mental state is in direct conflict with highway safety. Even the slightest impairment in respiratory function under emergency conditions (when greater oxygen supply is necessary for performance) may be detrimental to safe driving.

3. There are many conditions that interfere with oxygen exchange and may result in incapacitation, including emphysema, chronic asthma, carcinoma, tuberculosis, chronic bronchitis and sleep apnea. If the medical examiner detects a respiratory dysfunction, that in any way is likely to interfere with the driver’s ability to safely control and drive a commercial motor vehicle, the driver must be referred to a specialist for further evaluation and therapy. Anticoagulation therapy for deep vein thrombosis and/or pulmonary thromboembolism is not medically disqualifying once optimum dose is achieved, provided lower extremity venous examinations remain normal and the treating physician gives a favorable recommendation.

F. Hypertension: §391.41(b)(6)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no current clinical diagnosis of high blood pressure likely to interfere with ability to operate a commercial motor vehicle safely.

2. Hypertension alone is unlikely to cause sudden collapse; however, the likelihood increases when target organ damage, particularly cerebral vascular disease, is present. This regulatory criteria is based on the Federal Motor Carrier Safety Administration’s Cardiovascular Advisory Guidelines for the Examination of commercial motor vehicle Drivers, which used the Sixth Report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Pressure (1997).

3. Stage 1 hypertension corresponds to a systolic blood pressure of 140-159 mmHg and/or a diastolic blood pressure of 90-99 mmHg. The driver with a blood pressure in this range is at low risk for hypertension-related acute incapacitation and may be medically certified to drive for a one-year period. Certification examinations should be done annually thereafter and should be at or less than 140/90. If less than 160/100, certification may be extended one time for 3 months.

4. A blood pressure of 160-179 systolic and/or 100-109 diastolic is considered Stage 2 hypertension, and the driver is not necessarily unqualified during evaluation and institution of treatment. The driver is given a one-time certification of three months to reduce his or her blood pressure to less than or equal to 140/90. A blood pressure in this range is an absolute indication for anti-hypertensive drug therapy. Provided treatment is well tolerated and the driver demonstrates a blood pressure value of 140/90 or less, he or she may be certified for one year from date of the initial exam. The driver is certified annually thereafter.

5. A blood pressure at or greater than 180 (systolic) and 110 (diastolic) is considered Stage 3, high risk for an acute blood pressure-related event. The driver may not be qualified, even temporarily, until reduced to 140/90 or less and treatment is well tolerated. The driver may be certified for 6 months and biannually (every 6 months) thereafter if at recheck blood pressure is 140/90 or less.

6. Annual recertification is recommended if the medical examiner does not know the severity of hypertension prior to treatment. An elevated blood pressure finding should be confirmed by at least two subsequent measurements on different days.

7. Treatment includes nonpharmacologic and pharmacologic modalities as well as counseling to reduce other risk factors. Most antihypertensive medications also have side effects, the importance of which must be judged on an individual basis. Individuals must be alerted to the hazards of these medications while driving. Side effects of somnolence or syncope are particularly undesirable in commercial motor vehicle drivers.

8. Secondary hypertension is based on the above stages. Evaluation is warranted if patient is persistently hypertensive on maximal or near-maximal doses of 2-3 pharmacologic agents. Some causes of secondary hypertension may be amenable to surgical intervention or specific pharmacologic disease.

G. Rheumatic, Arthritic, Orthopedic, Muscular, Neuromuscular or Vascular Disease: §391.41(b)(7)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no established medical history or clinical diagnosis of rheumatic, arthritic, orthopedic, muscular, neuromuscular or vascular disease which interferes with the ability to control and operate a commercial motor vehicle safely.

2. Certain diseases are known to have acute episodes of transient muscle weakness, poor muscular coordination (ataxia), abnormal sensations (paresthesia), decreased muscular tone (hypotonia), visual disturbances and pain which may be suddenly incapacitating. With each recurring episode, these symptoms may become more pronounced and remain for longer periods of time. Other diseases have more insidious onsets and display symptoms of muscle wasting (atrophy), swelling and paresthesia which may not suddenly incapacitate a person but may restrict his/her movements and eventually interfere with the ability to safely operate a motor vehicle. In many instances these diseases are degenerative in nature or may result in deterioration of the involved area.

3. Once the individual has been diagnosed as having a rheumatic, arthritic, orthopedic, muscular, neuromuscular or vascular disease, then he/she has an established history of that disease. The physician, when examining an individual, should consider the following: The nature and severity of the individual’s condition (such as sensory loss or loss of strength); the degree of limitation present (such as range of motion); the likelihood of progressive limitation (not always present initially but may manifest itself over time); and the likelihood of sudden incapacitation. If severe functional impairment exists, the driver does not qualify. In cases where more frequent monitoring is required, a certificate for a shorter period of time may be issued.

H. Epilepsy: §391.41(b)(8)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no established medical history or clinical diagnosis of epilepsy or any other condition which is likely to cause loss of consciousness or any loss of ability to control a motor vehicle.

2. Epilepsy is a chronic functional disease characterized by seizures or episodes that occur without warning, resulting in loss of voluntary control which may lead to loss of consciousness and/or seizures. Therefore, the following drivers cannot be qualified:

(i) A driver who has a medical history of epilepsy;

(ii) A driver who has a current clinical diagnosis of epilepsy; or

(ii) A driver who is taking antiseizure medication.

3. If an individual has had a sudden episode of a nonepileptic seizure or loss of consciousness of unknown cause which did not require antiseizure medication, the decision as to whether that person’s condition will likely cause loss of consciousness or loss of ability to control a motor vehicle is made on an individual basis by the medical examiner in consultation with the treating physician. Before certification is considered, it is suggested that a 6 month waiting period elapse from the time of the episode. Following the waiting period, it is suggested that the individual have a complete neurological examination. If the results of the examination are negative and antiseizure medication is not required, then the driver may be qualified.

4. In those individual cases where a driver has a seizure or an episode of loss of consciousness that resulted from a known medical condition (e.g., drug reaction, high temperature, acute infectious disease, dehydration or acute metabolic disturbance), certification should be deferred until the driver has fully recovered from that condition and has no existing residual complications, and not taking antiseizure medication.

5. Drivers with a history of epilepsy/seizures off antiseizure medication and seizure-free for 10 years may be qualified to drive a commercial motor vehicle in interstate commerce. Interstate drivers with a history of a single unprovoked seizure may be qualified to drive a commercial motor vehicle in interstate commerce if seizure-free and off antiseizure medication for a 5-year period or more.

I. Mental Disorders: §391.41(b)(9)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no mental, nervous, organic or functional disease or psychiatric disorder likely to interfere with ability to drive a motor vehicle safely.

2. Emotional or adjustment problems contribute directly to an individual’s level of memory, reasoning, attention, and judgment. These problems often underlie physical disorders. A variety of functional disorders can cause drowsiness, dizziness, confusion, weakness or paralysis that may lead to incoordination, inattention, loss of functional control and susceptibility to accidents while driving. Physical fatigue, headache, impaired coordination, recurring physical ailments and chronic “nagging” pain may be present to such a degree that certification for commercial driving is inadvisable. Somatic and psychosomatic complaints should be thoroughly examined when determining an individual’s overall fitness to drive. Disorders of a periodically incapacitating nature, even in the early stages of development, may warrant disqualification.

3. Many bus and truck drivers have documented that “nervous trouble” related to neurotic, personality, or emotional or adjustment problems is responsible for a significant fraction of their preventable accidents. The degree to which an individual is able to appreciate, evaluate and adequately respond to environmental strain and emotional stress is critical when assessing an individual’s mental alertness and flexibility to cope with the stresses of commercial motor vehicle driving.

4. When examining the driver, it should be kept in mind that individuals who live under chronic emotional upsets may have deeply ingrained maladaptive or erratic behavior patterns. Excessively antagonistic, instinctive, impulsive, openly aggressive, paranoid or severely depressed behavior greatly interfere with the driver’s ability to drive safely. Those individuals who are highly susceptible to frequent states of emotional instability (schizophrenia, affective psychoses, paranoia, anxiety or depressive neuroses) may warrant disqualification. Careful consideration should be given to the side effects and interactions of medications in the overall qualification determination.

J. [Reserved]

K. Hearing: §391.41(b)(11)

1. A person is physically qualified to drive a commercial motor vehicle if that person: First perceives a forced whispered voice in the better ear at not less than 5 feet with or without the use of a hearing aid, or, if tested by use of an audiometric device, does not have an average hearing loss in the better ear greater than 40 decibels at 500 Hz, 1,000 Hz, and 2,000 Hz with or without a hearing aid when the audiometric device is calibrated to American National Standard (formerly ADA Standard) Z24.5-1951.

2. Since the prescribed standard under the Federal Motor Carrier Safety Regulations is from the American National Standards Institute, formerly the American Standards Association, it may be necessary to convert the audiometric results from the International Organization for Standardization standard to the American National Standards Institute standard. Instructions are included on the Medical Examination Report Form.

3. If an individual meets the criteria by using a hearing aid, the driver must wear that hearing aid and have it in operation at all times while driving. Also, the driver must be in possession of a spare power source for the hearing aid.

4. For the whispered voice test, the individual should be stationed at least 5 feet from the medical examiner with the ear being tested turned toward the medical examiner. The other ear is covered. Using the breath which remains after a normal expiration, the medical examiner whispers words or random numbers such as 66, 18, 3, etc. The medical examiner should not use only sibilants (s sounding materials). The opposite ear should be tested in the same manner.

5. If the individual fails the whispered voice test, the audiometric test should be administered. If an individual meets the criteria by the use of a hearing aid, the following statement must appear on the Medical Examiner’s Certificate “Qualified only when wearing a hearing aid.”

L. Drug Use: §391.41(b)(12)

1. A person is physically qualified to drive a commercial motor vehicle if that person does not use any drug or substance identified in 21 CFR 1308.11, an amphetamine, a narcotic, or other habit-forming drug. A driver may use a non-Schedule I drug or substance that is identified in the other Schedules in 21 CFR part 1308 if the substance or drug is prescribed by a licensed medical practitioner who:

(i) Is familiar with the driver’s medical history, and assigned duties; and

(ii) Has advised the driver that the prescribed substance or drug will not adversely affect the driver’s ability to safely operate a commercial motor vehicle.

2. This exception does not apply to methadone. The intent of the medical certification process is to medically evaluate a driver to ensure that the driver has no medical condition which interferes with the safe performance of driving tasks on a public road. If a driver uses an amphetamine, a narcotic or any other habit-forming drug, it may be cause for the driver to be found medically unqualified. If a driver uses a Schedule I drug or substance, it will be cause for the driver to be found medically unqualified. Motor carriers are encouraged to obtain a practitioner’s written statement about the effects on transportation safety of the use of a particular drug.

3. A test for controlled substances is not required as part of this biennial certification process. The Federal Motor Carrier Safety Administration or the driver’s employer should be contacted directly for information on controlled substances and alcohol testing under Part 382 of the FMCSRs.

4. The term “uses” is designed to encompass instances of prohibited drug use determined by a physician through established medical means. This may or may not involve body fluid testing. If body fluid testing takes place, positive test results should be confirmed by a second test of greater specificity. The term “habit-forming” is intended to include any drug or medication generally recognized as capable of becoming habitual, and which may impair the user’s ability to operate a commercial motor vehicle safely.

5. The driver is medically unqualified for the duration of the prohibited drug(s) use and until a second examination shows the driver is free from the prohibited drug(s) use. Recertification may involve a substance abuse evaluation, the successful completion of a drug rehabilitation program, and a negative drug test result. Additionally, given that the certification period is normally two years, the medical examiner has the option to certify for a period of less than 2 years if this medical examiner determines more frequent monitoring is required.

M. Alcoholism: §391.41(b)(13)

1. A person is physically qualified to drive a commercial motor vehicle if that person: Has no current clinical diagnosis of alcoholism.

2. The term “current clinical diagnosis of” is specifically designed to encompass a current alcoholic illness or those instances where the individual’s physical condition has not fully stabilized, regardless of the time element. If an individual shows signs of having an alcohol-use problem, he or she should be referred to a specialist. After counseling and/or treatment, he or she may be considered for certification.

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Most Recent Highlights In Environmental

Final rule adds EtO emission limits to polyether polyol production
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Final rule adds EtO emission limits to polyether polyol production

The Environmental Protection Agency (EPA) finalized major changes to the National Emission Standards for Hazardous Air Pollutants (NESHAP) for Polyether Polyols (PEPO) Production (PEPO NESHAP).

Who’s impacted?

The final rule applies to facilities that produce polyether polyols and are subject to the regulations at 40 CFR 63 Subpart PPP.

What are the changes?

EPA’s final rule establishes ethylene oxide (EtO) standards, updates maximum achievable control technology (MACT) requirements, and revises other provisions for the PEPO NESHAP.

EtO standards

The final rule adds EtO emission standards for:

  • Equipment leaks,
  • Heat exchange systems,
  • Process vents,
  • Storage vessels, and
  • Wastewater.

The standards set emission limits and add requirements for monitoring and leak repairs.

MACT standards

Further, the final rule:

  • Requires heat exchange systems to use the more sensitive Modified El Paso Method (also known as the Air Stripping Method) for quarterly monitoring and a leak definition of 6.2 parts per million by volume of total strippable hydrocarbon concentration (as methane) in the stripping gas,
  • Lowers the MACT control thresholds for batch process vents and storage vessels,
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  • Lowers the threshold for equipment leaks for valves in gas/vapor service or light liquid service, and
  • Requires transfer operations with loading operations that exceed a certain threshold to use a vapor balance system or reduce emissions.

Other standards

EPA’s final rule also:

  • Requires 5-year performance testing for process vent control devices;
  • Revises flare monitoring and operational requirements to ensure they meet the MACT standards at all times when controlling hazardous air pollutant (HAP) emissions;
  • Adds new monitoring requirements for pressure vessels to verify that no detectable emissions exist;
  • Clarifies that any bypass of a pollution control device for closed vent systems is a violation;
  • Aligns the requirements for surge control vessels and bottoms receivers with the process vent standards;
  • Adds butylene oxide to the definition of “epoxide” and the HAPs list;
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  • Finalizes work practice standards for maintenance vents and equipment openings, storage vessel degassing, and routine storage vessel maintenance.

However, EPA didn’t finalize the 2024 proposed rule’s addition of a fenceline monitoring program for EtO or its changes to the continuous process vent standard.

What’s the compliance timeline?

Facilities subject to the PEPO NESHAP must comply with the changes by March 18, 2029, or upon startup, whichever is later.

Key to remember: EPA’s final rule for polyether polyol emissions makes significant changes, such as establishing EtO limits and revising MACT standards.

Key questions in industrial stormwater compliance
2026-03-16T05:00:00Z

Key questions in industrial stormwater compliance

Industrial stormwater compliance can feel complex for facilities balancing operations, employees, and shifting permit requirements. Many questions center on the federal general permit, pollution prevention plan expectations, monitoring, and what to do in everyday situations where stormwater risks arise. The following sections summarize core topics and practical concerns.

What is the current status of the federal 2021 Multi-Sector General Permit (MSGP)?

EPA issued the current MSGP in 2021, and it remains in effect beyond its February 28, 2026 expiration until EPA finalizes the proposed 2026 MSGP. Because the proposed 2026 permit is still under review, the 2021 MSGP continues to govern covered facilities.

Why has the proposed 2026 MSGP not taken effect?

EPA released the proposed 2026 MSGP in December 2024. Public comments, including an extended comment period ending May 19, 2025, must be reviewed before finalizing the permit. Since the existing MSGP remains valid until replaced, the 2021 permit stays in force while EPA completes its process.

What is a Stormwater Pollution Prevention Plan (SWPPP)?

A SWPPP outlines how a facility prevents pollutants from reaching stormwater. It identifies pollutant sources, control measures, inspection routines, monitoring steps, and staff training. A SWPPP must be written before submitting a Notice of Intent (NOI) for permit coverage and updated when operations or stormwater risks change.

What are the requirements for authorized state stormwater permits?

Most states issue their own industrial stormwater permits modeled on the federal MSGP. These permits typically require:

  • Preparation and maintenance of a SWPPP;
  • Inspections and monitoring (such as benchmark, effluent, or visual monitoring);
  • Corrective actions when control measures fail; and
  • Reporting through state online systems.

States may add requirements based on local conditions. When EPA updates the MSGP, states often revise their permits to align with new federal standards.

Who needs coverage under the MSGP?

Industrial facilities that discharge stormwater to waters of the United States generally need permit coverage unless they qualify for a no‑exposure exclusion. The federal MSGP applies in areas where EPA, not the state, holds National Pollutant Discharge Elimination System (NPDES) authority.

How does a facility obtain coverage?

To obtain coverage, a facility must:

  • Prepare and implement a SWPPP;
  • Put pollution controls in place, such as good housekeeping and spill prevention;
  • Identify sector specific requirements based on the permit; and
  • Submit a Notice of Intent through EPA’s online system.

The proposed 2026 MSGP includes updated forms and appendices, but current requirements remain based on the 2021 version until a new permit is published.

What monitoring is required?

Under the 2021 MSGP, required monitoring may include:

  • Quarterly visual assessments,
  • Benchmark monitoring in designated years, and
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The proposed 2026 MSGP would expand per- and polyfluoroalkyl substances (PFAS) sampling, increase benchmark monitoring frequency, and add requirements for impaired waters. These changes remain pending.

What happens if benchmark thresholds are exceeded?

A benchmark exceedance requires the facility to investigate causes, improve control measures, and document actions in the SWPPP. The proposed 2026 MSGP would formalize additional implementation measures and reporting steps, but these wouldn’t apply until the new permit takes effect.

What about common real world compliance scenarios?

Industrial stormwater issues often arise from everyday activities. Consider these examples:

Employees’ vehicles leaking oil in parking lots

Leaks from employee vehicles can contaminate stormwater. While the MSGP does not regulate personal vehicles directly, the facility is responsible for any pollutants that enter stormwater from its property. Good housekeeping practices include absorbent stations, spill kits, drip pans, and designated parking areas with routine inspection.

Nonroutine outdoor maintenance

Temporary outdoor activities such as conducting maintenance, unloading equipment, or staging materials, can introduce pollutants. The SWPPP should address nonroutine tasks by requiring temporary controls like tarps, containment pads, or scheduling activities during dry weather. Documentation of these activities is also part of good recordkeeping.

Outdoor waste storage or scrap piles

These materials should be covered or sheltered, kept away from storm drains, and inspected frequently. If runoff contacts industrial materials, the discharge becomes regulated and must be managed under the permit.

These scenarios reinforce the need for strong housekeeping practices, staff training, and prompt corrective actions.

What documentation must facilities keep?

Facilities must maintain monitoring records, inspection logs, SWPPP updates, and corrective action reports. EPA may request these documents at any time. Appendices in the proposed 2026 MSGP preview updated forms, but the 2021 requirements remain in place for now.

What should facilities do while waiting for the 2026 MSGP?

Facilities should continue full compliance with the 2021 MSGP, track regulatory updates, and prepare for more frequent monitoring and PFAS sampling likely included in the 2026 permit. Reviewing proposed changes now helps facilities plan needed SWPPP updates in advance.

Key to remember: Industrial facilities covered under the 2021 MSGP or a state equivalent must continue following that permit until EPA issues a new federal MSGP. Staying informed, maintaining strong housekeeping, and keeping SWPPP documentation current remain the most effective strategies for compliance.

Toxics Release Inventory: Are you ready to report?
2026-03-13T05:00:00Z

Toxics Release Inventory: Are you ready to report?

Every year at the beginning of July, industrial facilities across the nation can breathe a collective sigh of relief — their annual inventories of toxic chemicals are complete! To ensure that your facility can be part of that celebration (and avoid a chaotic rush to meet the deadline), now’s the perfect time to start preparing for the Toxics Release Inventory (TRI).

The Environmental Protection Agency’s (EPA’s) TRI program requires industrial facilities to report waste management data on certain toxic chemicals they manufacture, process, and use by July 1 each year. Is your facility ready to report? Here’s an overview of the TRI program to help you answer this question.

Who’s covered by TRI reporting?

Generally, TRI reporting applies if the facility:

  • Is in a covered industry sector (40 CFR 372.23);
  • Employs 10 or more full-time-equivalent employees; and
  • Manufactures, processes, or otherwise uses a covered chemical or chemical category (372.65) in quantities above the threshold levels (372.25, .27, and .28) in a given year.

TRI tip: The TRI reporting year (RY) reflects the calendar year covered by the report, not the year in which you submit the report. For example, TRI reports for RY 2025 are due by July 1, 2026.

What’s covered by TRI reporting?

Facilities must submit the TRI Form R (or the streamlined Form A Certification Statement if eligible) for each TRI-listed chemical manufactured, processed, or used during the previous calendar year. The data covers chemical waste management activities (including releases to the environment) and any actions taken to reduce or prevent chemical waste.

Facilities usually report for each chemical:

  • The quantities of releases (routine and accidental),
  • Any releases caused by catastrophic or other one-time events,
  • The maximum amount on-site during the year, and
  • The amount contained in wastes managed on-site or transferred off-site.

What’s new for RY 2025?

The TRI reports for RY 2025 contain three differences from previous years:

  • The de minimis level for anthracene was lowered from 1.0 percent to 0.1 percent. Anthracene’s Chemical Abstracts Service Registry Number (CASRN) is 120-12-7.
  • More activity sub-use codes were added to the sub-use codes for “processing” and “otherwise use” activities.
  • Nine per- and polyfluoroalkyl substances (PFAS) were added to the TRI chemical list:

EPA registry nameCASRN
6:2 fluorotelomer sulfonate acid27619-97-2
6:2 fluorotelomer sulfonate ammonium salt59587-39-2
6:2 fluorotelomer sulfonate anion425670-75-3
6:2 fluorotelomer sulfonate potassium salt59587-38-1
6:2 fluorotelomer sulfonate sodium salt27619-94-9
Acetic acid, [(.gamma.-.omega.-perfluoro-C8-10-alkyl)thio] derivs., Bu esters3030471-22-5
Ammonium perfluorodecanoate3108-42-7
Perfluoro-3-methoxypropanoic acid377-73-1
Sodium perfluorodecanoate3830-45-3

How are TRI reports submitted?

Facilities must submit TRI reports electronically to the TRI-MEweb application on EPA’s Central Data Exchange (CDX). Even if a facility uses its own software to prepare TRI forms, it must upload and submit the forms to TRI-MEweb.

TRI tip: To complete the submission process on TRI-MEweb, you need to assign one user the Preparer role and another user the Certifying Official role. Ensure both users have added TRI-MEweb to their CDX user accounts.

TRI reports must be submitted to both EPA and the state. If your facility’s state participates in the TRI Data Exchange (TDX), TRI-MEweb will automatically send your report to the state. If your facility’s state doesn’t participate, you must send a hard copy of the report to the TRI state contact.

TRI tip: Use EPA’s “TRI Data Exchange” webpage to determine whether your facility’s state participates in TDX. As of March 2026, all 50 states participate in TDX. The District of Columbia doesn’t participate.

More TRI tips

Keep these things in mind when preparing your TRI reports:

  • You must submit a Form R (or Form A if eligible) for each TRI-listed chemical your facility manufactured, processed, or otherwise used above the threshold quantity.
  • TRI data is publicized. If a chemical’s identity needs to be protected, you have to submit substantiation forms to claim the chemical identity as a trade secret. EPA must approve the claims. Further, for each chemical with a trade secret claim, you have to mail hard copies of the substantiation forms and the corresponding Form R (or Form A if eligible) to EPA and the state.
  • EPA’s online GuideME platform offers comprehensive guidance for TRI reporting, including reporting forms and instructions, the TRI chemical list, and Q&As.
  • Contact the state environmental agency directly to confirm the submission method. EPA’s “TRI State Contacts” webpage contains state contact information.
  • Register your facility on CDX or ensure your facility’s CDX account is updated as soon as possible to avoid delays caused by technical issues.

Start preparing for TRI reporting now to give your facility plenty of time to gather data, complete the forms, and respond to unexpected issues that could arise. That way, your facility can breathe easily throughout the whole reporting season.

Key to remember: The submission deadline for TRI reporting is July 1, 2026. Make sure your facility is ready to report.

EPA finalizes emission standards for large municipal waste combustors
2026-03-12T05:00:00Z

EPA finalizes emission standards for large municipal waste combustors

On March 10, 2026, the Environmental Protection Agency (EPA) finalized emission regulations for large municipal waste combustors (LMWCs). The final rule revises nearly all emission limits for new and existing LMWCs.

Who’s impacted?

The final rule applies to LMWCs that combust more than 250 tons per day of municipal solid waste and are covered by the:

  • New Source Performance Standards (NSPS) for new LMWCs, or
  • Emission Guidelines (EGs) for existing LMWCs.

EPA established new subparts for the amendments at 40 CFR Part 60, including:

  • Subpart VVVV for the NSPS, and
  • Subpart WWWW for the EGs.

What are the changes?

Generally, stricter emission limits apply. For all LMWCs (new and existing), the rule revises the emission limits for:

  • Cadmium,
  • Hydrogen chloride,
  • Lead,
  • Mercury,
  • Particulate matter,
  • Polychlorinated dibenzodioxins and dibenzofurans, and
  • Sulfur dioxide.

For all new LMWCs, the final rule revises the emission limits for carbon monoxide (CO) and nitrogen oxides (NOx). The final rule also amends the CO and NOx limits for all existing LMWCs, except for the CO limits for two subcategories of combustors and the NOx limits for two subcategories of combustors for new municipal solid waste incinerators.

Other major changes include:

  • Removing certain exclusions and exemptions for startups, shutdowns, and malfunctions (requiring LMWCs to meet emission standards at all times);
  • Removing the NOx emissions averaging compliance alternative for existing LMWCs;
  • Amending recordkeeping and reporting requirements; and
  • Eliminating Title V operating air permit requirements for qualifying air curtain incinerators that burn only wood waste, yard waste, and clean lumber.

What’s the compliance timeline?

When EPA updates EGs, states must revise their State Implementation Plans (SIPs) to incorporate the changes. States have to submit revised SIPs by March 10, 2027. Once EPA approves the SIP, facilities with existing LMWCs must meet the new standards either within 3 years of the SIP’s approval date or by March 10, 2031, whichever is earlier.

New LMWCs must comply with the amended NSPS by September 10, 2026, or upon startup, whichever is later.

Key to remember: EPA finalized stronger emission limits for new and existing large municipal waste combustors and made other changes to the standards.

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!

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Most Recent Highlights In Transportation

2026-03-06T06:00:00Z

Colorado adds landfill methane emission regulation

Effective date: February 14, 2026

This applies to: Open and closed municipal solid waste landfills

Description of change: The Colorado Air Quality Control Commission added Regulation 31, which establishes new emission control and monitoring requirements for municipal solid waste landfills. Applicability is based on the landfill’s amount of waste it holds and methane emissions.

Significant changes implemented by Regulation 31 include:

  • Establishing a stricter emission control threshold than federal standards so that more landfills must install gas collection and control systems,
  • Mandating closed landfills with emission combustion devices to install biofilters when the devices are removed,
  • Expanding the methane monitoring requirements (allowing additional monitoring tools for identifying large emission sources) and allowing alternative monitoring technologies for periodic monitoring, and
  • Phasing in a ban on open flares to replace them with enclosed flares.

Related state info: Clean air operating permits state comparison

2026-03-06T06:00:00Z

Louisiana amends Voluntary Environmental Self-Audit Program

Effective date: January 20, 2026

This applies to: Participating entities

Description of change: The Louisiana Department of Environmental Quality (LDEQ) revised the Voluntary Environmental Self-Audit Program rules in January 2026. Some of the changes include:

  • Adding definitions,
  • Changing the timeline to notify LDEQ of violations from 45 days within discovery to 30 days after the end of the audit, and
  • Requiring participants to submit monthly progress reports if corrective actions take longer than 90 days.
2026-03-06T06:00:00Z

Delaware revises 2026 NPDES general construction permit

Effective date: March 11, 2026

This applies to: Construction activities that discharge stormwater into Waters of the State

Description of change: The Delaware Department of Natural Resources and Environmental Control (DNREC) revised the Delaware National Pollutant Discharge Elimination System (NPDES) Construction General Permit (CGP), which implements the DNREC Sediment and Stormwater Management Program.

It applies to construction activities that plan to disturb 1 or more acres (or activities that plan to disturb less than 1 acre but are part of a larger common plan of development or sale that will disturb more than 1 acre) that discharge stormwater to Waters of the State.

The DNREC made minimal changes to the NPDES CGP. The 2026 NPDES CGP will provide coverage for 5 years.

Related state info: Construction water permitting — Delaware

2026-03-06T06:00:00Z

California updates water diversion regulations

Effective date: February 1, 2026

This applies to: Water right holders who divert more than 10 acre-feet per year

Description of change: The California State Water Resources Control Board (SWRCB) updated the Water Measurement and Reporting Regulation (SB 88) with changes primarily affecting reporting requirements, such as:

  • Requiring diverters to submit data to the SWRCB using a template or the online reporting platform CalWATRS,
  • Requiring large diverters to submit data to CalWATRS instead of posting it to any public website,
  • Requiring diverters to identify and report measurement locations, and
  • Requiring diverters to submit their measurement methodologies.

Updated measuring and reporting requirements take effect on October 1, 2026.

EPA proposes electronic-only hazardous waste manifests
2026-03-06T06:00:00Z

EPA proposes electronic-only hazardous waste manifests

On March 5, 2026, the Environmental Protection Agency (EPA) issued a proposed rule to end the use of paper hazardous waste manifests and require waste handlers to use electronic manifests on the Hazardous Waste Electronic Manifest (e-Manifest) System to track all shipments of hazardous waste regulated under the Resource Conservation and Recovery Act (RCRA).

What are the proposed changes?

EPA proposes to “sunset” (i.e., phase out) the use of paper manifests and shift to using only electronic manifests (either fully electronic or hybrid) to track RCRA hazardous waste shipments.

The sunset compliance date would be 2 years from the publication date of a final rule. On and after the sunset compliance date, EPA would no longer accept paper hazardous waste manifests (image-only and data-plus-image submission types). In other words, regulated waste handlers would have to use fully electronic or hybrid manifests on the e-Manifest System for all hazardous waste shipments initiated on and after the sunset compliance date.

Who would be impacted?

The proposed rule would affect waste handlers involved in manifesting hazardous waste, including:

  • Generators,
  • Transporters, and
  • Receiving facilities.

Many of the proposed changes would align RCRA regulations with the shift to electronic-only manifesting and with the 2024 e-Manifest Third Rule’s changes. The proposed rule also contains technical corrections to import and export regulations.

Additionally, EPA’s proposed rule would add requirements for:

  • Very small quantity generators (VSQGs) managing episodic events,
  • RCRA hazardous waste transporters,
  • Healthcare facilities and reverse distributors subject to RCRA’s hazardous waste pharmaceutical requirements,
  • Certain polychlorinated biphenyl (PCB) waste generators,
  • PCB waste transporters, and
  • Hazardous waste treatment or storage facilities with standardized RCRA permits.

Examples of these requirements include:

  • Mandating specific waste handlers to register with the e-Manifest System;
  • Requiring VSQGs, healthcare facilities, and reverse distributors to submit data corrections to the e-Manifest System within 30 days of a request from EPA or an authorized state; and
  • Requiring hazardous waste generators and PCB waste generators to identify brokers on the manifest.

EPA will accept public comments on the proposed rule (Docket ID No. EPA-HQ-OLEM-2025-3456) through May 4, 2026.

Key to remember: EPA proposes to end the use of paper manifests and require waste handlers to use electronic manifests to track all RCRA hazardous waste shipments.

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Most Recent Highlights In Safety & Health

EPA temporarily extends 2021 MSGP coverage
2026-03-04T06:00:00Z

EPA temporarily extends 2021 MSGP coverage

The Environmental Protection Agency (EPA) has issued an administrative continuance of the 2021 Multi-Sector General Permit (MSGP) and a No Action Assurance memorandum for industrial stormwater discharges regulated under the National Pollutant Discharge Elimination System.

The 2021 MSGP expired on February 28, 2026. However, because EPA hasn’t reissued a new permit to replace the expired permit, the 2021 MSGP remains in effect for facilities previously covered. Additionally, the No Action Assurance allows facilities without previous coverage to discharge industrial stormwater in compliance with the 2021 MSGP.

Who’s affected?

Facilities are required to obtain MSGPs for stormwater discharges from industrial activities in areas where EPA is the permitting authority, including:

  • Existing facilities (those that had active coverage under the 2021 MSGP), and
  • New facilities (those that didn’t obtain coverage under the 2021 MSGP before it expired).

What do existing facilities do?

The administrative continuance automatically applies to existing facilities that were actively covered by the 2021 MSGP before it expired. The facility’s coverage status should show “Admin. Continued” in the NPDES eReporting Tool (NeT-MSGP).

Facilities will remain covered by the 2021 MSGP until EPA issues a new MSGP and the facilities obtain coverage under the new MSGP. Until then, existing facilities should continue to comply with the 2021 MSGP requirements.

EPA will provide further guidance on renewing coverage when it issues the new MSGP.

What do new facilities do?

New facilities can’t obtain coverage under the MSGP until EPA issues a new permit. However, EPA issued a memorandum on February 27, 2026, establishing a No Action Assurance. The agency won’t take enforcement action against new facilities for unpermitted stormwater discharges if the facilities meet specific conditions.

The No Action Assurance extends from March 1, 2026, to the new MSGP’s effective date.

Applicability

EPA’s No Action Assurance applies to facilities that:

  • Discharge stormwater on or after March 1, 2026 (but before the new MSGP’s effective date); and
  • Didn’t submit a Notice of Intent (NOI) for coverage under the 2021 MSGP before its expiration on February 28, 2026.

The assurance doesn’t apply to existing facilities that started stormwater discharges before February 28, 2026, without obtaining 2021 MSGP coverage.

Conditions

To be covered by the No Action Assurance, new facilities have to:

  • Meet the 2021 MSGP eligibility criteria,
  • Submit an NOI form (Appendix G of the MSGP) via msgp@epa.gov to notify EPA of their intention to operate according to all applicable 2021 MSGP requirements before discharging industrial stormwater, and
  • Comply with all applicable 2021 MSGP regulations, such as:
    • Developing and implementing a Stormwater Pollution Prevention Plan,
    • Installing and maintaining stormwater controls, and
    • Conducting site inspections and monitoring.

What’s next?

Once EPA issues the new MSGP, facilities planning to continue industrial stormwater discharges must submit a new NOI through Net-MSGP within 90 days of the new MSGP’s effective date to obtain coverage under the new MSGP.

EPA provides guidance for existing and new facilities on its “Administrative Continuance of EPA’s 2021 MSGP” webpage.

Key to remember: EPA has temporarily extended coverage under the 2021 MSGP for industrial stormwater discharges until the agency issues a new general permit.

EPA extends 2025 GHG reporting deadline
2026-02-27T06:00:00Z

EPA extends 2025 GHG reporting deadline

The Environmental Protection Agency (EPA) finalized a rule on February 27, 2026, extending the submission deadline for the 2025 annual greenhouse gas (GHG) report from March to October 2026.

Who’s impacted?

The final rule applies to facilities regulated by the GHG Reporting Program (GHGRP) at 40 CFR Part 98. Generally, the GHGRP’s annual reporting requirement applies to three types of reporters:

  • Large industrial sources of GHG emissions (that directly emit 25,000 or more metric tons of carbon dioxide equivalent (CO2e) per year);
  • Fuel and industrial gas suppliers (whose products would result in 25,000 or more metric tons of CO2e of GHG emissions per year if released, combusted, or oxidized); and
  • CO2 injection facilities (that receive 25,000 or more metric tons of CO2 for injection).

What’s the change?

The final rule extends the submission deadline for the reporting year (RY) 2025 annual GHG report from March 31, 2026, to October 30, 2026. The delay applies only to RY 2025.

EPA explains in the final rule that delaying the submission deadline for the RY 2025 GHG report gives the agency time to take final action on the proposed revisions to the GHGRP (published in September 2025).

What does the GHG report cover?

The GHGRP requires facilities to report GHG data and other related information covering the previous calendar year.

The subparts under Part 98 contain the reporting requirements, and regulated facilities must report emissions for all applicable source categories. Reporters must use specific methods to calculate GHG emissions, which are detailed in the regulations; they can usually choose from a collection of methods.

Key to remember: EPA’s final rule delays the submission deadline for the 2025 annual GHG report from March to October 2026.

EPA scraps Endangerment Finding, GHG emission standards: What you need to know
2026-02-25T06:00:00Z

EPA scraps Endangerment Finding, GHG emission standards: What you need to know

“Road Closed Ahead.” That’s the sign that now stands at the entrance of the regulatory road leading to the federal greenhouse gas (GHG) emission standards for vehicle and engine manufacturers.

The Environmental Protection Agency (EPA) finalized a rule on February 18, 2026, to rescind the 2009 Endangerment Finding and repeal all GHG emission standards for new motor vehicles and motor vehicle engines. The final rule applies to vehicles and engines of model years (MYs) 2012 to 2027 and beyond.

This overview will help you navigate EPA’s final rule that puts vehicle GHG emission requirements in the rearview mirror.

What does this mean?

Manufacturers (including importers) of motor vehicles and motor vehicle engines no longer have future obligations to measure, control, report, or comply with federal GHG emission standards for any highway vehicle or engine, including for previously manufactured MYs.

Specifically, the final rule removes the requirements for controlling GHG emissions, which include:

  • Emission standards;
  • Test procedures;
  • Averaging, banking, and trading requirements;
  • Reporting requirements; and
  • Fleet-average emission requirements.

Additionally, the final rule eliminates off-cycle credits for manufacturers that added certain technologies to their vehicles and engines (like waste heat recovery) and EPA’s incentives for manufacturers to install a start-stop system (which automatically shuts off a vehicle’s engine when idling).

When do the changes apply?

The final rule takes effect on April 20, 2026. However, a legal challenge has already been brought against the rulemaking, and more litigation is likely.

It’s important to keep an eye on the status of the rule. Legal challenges could result in changes to the rule, such as delaying its effective date.

What regulations were removed?

The final rule repeals all GHG emission regulations in 40 CFR:

Why did EPA remove the standards?

The road to reversal begins in 2009. That’s when EPA issued two findings: the Endangerment Finding and the Cause or Contribute Finding. Collectively, these findings are referred to as the 2009 Endangerment Finding. The agency used the 2009 Endangerment Finding as the legal basis under Section 202(a) of the Clean Air Act (CAA) to regulate GHG emissions from new motor vehicles and motor vehicle engines based on global climate change concerns.

However, upon reconsideration, EPA no longer believes that it has the statutory authority under Section 202(a) of the CAA to regulate GHG emissions from new motor vehicles and motor vehicle engines in response to global climate change concerns. The agency bases its determination on three factors:

  • EPA concludes that the best reading of Section 202(a) of the CAA authorizes the agency to regulate air pollution that threatens to endanger health and welfare through local and regional exposure. Therefore, the CAA doesn’t give EPA the authority to regulate GHG emissions based on global climate change concerns. The agency conducted the “best reading” by using standard interpretation principles and being informed by the Supreme Court’s overturning of “Chevron deference” in Loper Bright Enterprises v. Raimondo (2024).
  • EPA lacks the congressional authorization required to regulate GHG emissions based on global climate change concerns. The agency determined that the major questions doctrine (i.e., federal agencies may not decide issues of major national significance without clear authorization granted by Congress) applies to the Endangerment Finding and that Congress doesn’t give EPA the authority under Section 202(a) of the CAA to decide a national policy response to global climate change concerns.
  • The GHG emission regulations don’t and can’t have a meaningful impact on the identified health and welfare dangers that the Endangerment Finding attributed to global climate change. EPA based this conclusion on the results of climate impact modeling that the public submitted in response to the proposed rule and on the agency’s modeling analysis used to evaluate the submissions.

By rescinding the Endangerment Finding, EPA has no legal basis to regulate GHG emissions from new motor vehicles and motor vehicle engines. Accordingly, the final rule also repeals all GHG emission standards for light-, medium-, and heavy-duty vehicles and heavy-duty engines.

Key to remember: EPA’s final rule eliminates the 2009 Endangerment Finding and the related GHG emission requirements for on-highway vehicles and vehicle engines.

EPA repeals stricter Mercury and Air Toxics Standards for coal-, oil-fired power plants
2026-02-24T06:00:00Z

EPA repeals stricter Mercury and Air Toxics Standards for coal-, oil-fired power plants

On February 24, 2026, the Environmental Protection Agency (EPA) published a final rule repealing the 2024 amendments made to the National Emission Standards for Hazardous Air Pollutants (NESHAP) for Coal- and Oil-Fired Electric Utility Steam Generating Units (EGUs). It’s also referred to as the Mercury and Air Toxics Standards (MATS) for power plants.

Effective April 27, 2026, this rule (2026 Final Rule) repeals stricter compliance requirements made to the MATS rule in May 2024 (2024 Final Rule) and reverts them to the less stringent standards established by the 2012 MATS Rule.

Who’s affected?

The rule applies to power plants with coal- and oil-fired EGUs subject to the NESHAP (40 CFR 63 Subpart UUUUU).

What are the changes?

The final rule repeals these 2024 amendments:

  • The revised filterable particulate matter (fPM) emission standard and corresponding total and individual non-metal hazardous air pollutant (HAP) metal standards for existing coal-fired EGUs (reverting to the 2012 MATS Rule requirements);
  • The revised compliance demonstration requirements for all EGUs to install continuous emission monitoring systems (CEMS) for fPM emissions and the adjusted quality assurance criteria (reverting to the previous standard, allowing EGUs to choose from three compliance demonstration methods); and
  • The revised mercury (Hg) emission standard for lignite-fired EGUs (reverting to the 2012 MATS Rule limit).

The 2026 Final Rule also reinstates the low-emitting EGU (LEE) program for fPM and non-Hg HAP metals. The LEE program requires less frequent stack testing for sources with emissions below 50 percent of the corresponding limit for 3 consecutive years.

Further, EPA’s final rule updates the fPM sampling requirements for EGUs that demonstrate compliance with a PM CEMS. These units must collect either a minimum catch of 6.0 milligrams or a minimum sample volume of 4 dry standard cubic meters (dscm) per test run. EGUs demonstrating compliance using other methods must collect a lower minimum sample volume of 1 dscm per PM test run.

Compliance requirement2024 Final Rule2026 Final Rule
fPM emission limit for existing coal-fired EGUs0.010 pounds per million British thermal units of heat input (lb/MMBtu)0.030 lb/MMBTu
fPM emission compliance demonstration for all coal-and oil-fired EGUsEGUs must use PM CEMSEGUs may use:
  • Quarterly stack testing
  • PM continuous parametric monitoring systems
  • PM CEMS
Hg emission limit for existing lignite-fired EGUs1.2 pounds per trillion British thermal units of heat input (lb/TBtu)4.0 lb/TBtu
Key to remember: EPA’s final rule repeals the stricter emission limits set by the 2024 amendments to the Mercury and Air Toxics Standard for coal- and oil-fired power plants.
PFAS, pretreatment, and biosolids: The growing challenge for water permitting
2026-02-20T06:00:00Z

PFAS, pretreatment, and biosolids: The growing challenge for water permitting

Per and polyfluoroalkyl substances (PFAS) pose one of the most urgent and complex challenges for wastewater systems in the United States. As federal agencies reconsider their regulatory strategies and states impose their own standards, publicly owned treatment works (POTWs) and the industries that discharge to them face increasing pressure to control PFAS at the source. These pressures affect pretreatment permits, industrial dischargers, and biosolids management, forming a rapidly evolving compliance landscape. Recent federal assessments and state actions show that PFAS in wastewater and biosolids is no longer a distant regulatory issue. It is a primary driver shaping future POTW permitting.

PFAS in POTW systems: A problem that starts upstream

PFAS enter POTWs through a mix of industrial wastewater, landfill leachate, household products, and consumer goods. Because PFAS are persistent and resistant to conventional treatment, they pass through biological processes largely unchanged. This means industrial contributors sending PFAS to a POTW can cause downstream compliance problems, even at low concentrations. EPA has emphasized that the best way to manage PFAS in wastewater is to prevent the chemicals from entering treatment systems in the first place, placing new attention on upstream industrial sources.

EPA’s 2025 trajectory indicates broader PFAS rulemaking is coming under several environmental statutes, including the Clean Water Act (CWA), Resource Conservation and Recovery Act, and Safe Drinking Water Act, although the federal landscape remains in flux. Still, agencies agree on one point: pretreatment programs will be an essential component of PFAS control.

Pretreatment permits: The first line of defense

Pretreatment permits regulate indirect dischargers, meaning industrial facilities that send wastewater to POTWs instead of directly to surface waters. These permits already manage pollutants that interfere with treatment or pass through into receiving waters. Now, PFAS has become a central focus.

States and POTWs are increasingly requiring:

  • PFAS monitoring in industrial wastewater,
  • Source identification surveys,
  • Product substitution or process changes,
  • Best management practices to reduce PFAS at the facility, and
  • Local limits or prohibitions on PFAS discharges

EPA’s PFAS strategy specifically encourages states and POTWs to deploy all available pretreatment authorities to control PFAS at the source. This approach aligns with statements from EPA representatives asserting that upstream controls are one of the most effective tools for preventing PFAS from entering wastewater systems.

Biosolids under scrutiny: The impact of PFAS

The PFAS problem does not end with liquid effluent. It extends into biosolids, the treated sewage sludge generated by POTWs. In 2025, EPA released a Draft Sewage Sludge Risk Assessment evaluating risks associated with PFOS and PFOA in biosolids applied to land. The assessment found potential human health risks under certain scenarios when biosolid concentrations exceeded 1 part per billion. Although EPA emphasized the assessment is not a regulatory standard, many states immediately treated the value as a de facto limit for biosolid land application.

This rapid adoption has created a challenging environment for POTWs. Unless PFAS inputs from industrial sources are reduced, biosolid PFAS levels remain high, limiting disposal options such as:

  • Agricultural land application,
  • Composting,
  • Surface disposal,
  • Landfilling, and
  • Incineration

Some states have already implemented bans or strict standards on biosolid land application due to PFAS concerns.

Regulatory uncertainty adds pressure

EPA’s PFAS regulatory posture has shifted several times. In 2025, EPA announced its intent to rescind certain PFAS drinking water designations while maintaining standards for PFOS and PFOA, signaling continued reassessment of its overall PFAS approach. These actions underscore the unsettled nature of federal rulemaking.

Meanwhile, the 2021 PFAS Strategic Roadmap and its subsequent progress updates outline multiple forthcoming actions under the CWA, including potential effluent limitation guidelines (ELGs) for PFAS manufacturers and metal finishers. These ELGs, if finalized, would apply to industrial direct and indirect dischargers and shape pretreatment standards nationwide. Yet, as of early 2026, EPA has not finalized technology based effluent limits for PFAS nor established national PFAS biosolids requirements, leaving states to fill the regulatory void.

What POTWs and industrial users should do now

Despite uncertainty, actions today can reduce long term liability:

  • Conduct PFAS source identification at industrial users,
  • Require PFAS monitoring in pretreatment permits,
  • Develop local limits where state guidance is emerging,
  • Engage with industrial facilities early on substitution and pollution prevention,
  • Evaluate biosolids PFAS levels to assess disposal risks, and
  • Participate in state rulemaking to anticipate new limits

POTWs should also coordinate with state environmental agencies, which continue to implement PFAS restrictions independent of federal action.

Pretreatment programs and biosolids management are becoming central to U.S. PFAS compliance. POTWs sit at the intersection of regulatory expectations, industrial discharges, and community concerns. While federal PFAS rules remain in development, state actions and EPA’s strategic direction make one fact clear: controlling PFAS at the source is essential.

Key to remember: For both industrial users and POTWs, proactive PFAS management is no longer optional. It is a core element of future permitting, planning, and risk reduction.

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Most Recent Highlights In Human Resources

2026-02-13T06:00:00Z

Expert Insights: States take the lead as federal environmental rules pull back

Recent changes in federal environmental policy have created uncertainty for regulated industries. When federal agencies slow rulemaking, reduce enforcement, or narrow requirements, states often step in. As a result, states are taking a stronger role in setting environmental rules, especially on climate change, air quality, and environmental justice.

This shift is changing how industrial facilities understand and manage regulatory risks.

States as environmental policy leaders

Several states have moved to the front of environmental policymaking. California is the most well-known example. Through the California Air Resources Board (CARB), the state enforces air and climate rules that go beyond federal standards. These include strict vehicle emissions limits and greenhouse gas controls for industrial sources. Because California’s economy is so large, its rules often shape compliance decisions across the country.

Other states are following similar paths. For example, New York’s Climate Leadership and Community Protection Act sets clear, enforceable emissions-reduction goals. It also requires agencies to consider climate and environmental justice impacts during permitting. Washington has adopted a cap-and-invest program that limits carbon emissions from major sources and fuel suppliers.

Growing impacts on industrial facilities

For industrial operators, state-led regulation adds complexity and risk. Companies with facilities in multiple states may face very different rules, timelines, and reporting requirements. Meeting federal standards alone may no longer be enough.

Facilities can still fall out of compliance with state rules covering air emissions, water discharges, waste management, or community impacts. These differences can affect permitting schedules, capital planning, and long-term site decisions.

State enforcement and local focus

State enforcement is often more focused and, in many cases, more stringent than federal enforcement. Many states are increasing inspections and placing greater emphasis on environmental justice.

Facilities located near overburdened or historically impacted communities may face closer review, even when federal enforcement activity is limited.

Practical strategies for compliance

To operate successfully in this environment, companies need a proactive approach. Tracking state regulatory changes is essential, since states often move faster than federal agencies. Building compliance programs around the most stringent applicable rules can reduce long-term risk.

Early engagement with state regulators and local communities can also make a difference. Open communication can improve relationships, reduce conflict, and support smoother permitting outcomes.

For industrial facilities, success now depends less on watching Washington and more on understanding the growing influence of state capitals.

EPA reverses Endangerment Finding, scraps GHG emission standards for vehicles
2026-02-13T06:00:00Z

EPA reverses Endangerment Finding, scraps GHG emission standards for vehicles

The Environmental Protection Agency (EPA) published a final rule on February 18, 2026, to rescind the 2009 Endangerment Finding and repeal all federal greenhouse gas (GHG) emission standards for:

  • On-highway light-, medium-, and heavy-duty vehicles; and
  • On-highway heavy-duty vehicle engines.

The final rule takes effect on April 20, 2026, and applies to vehicles and engines of model years 2012 to 2027 and beyond.

What are the changes?

Manufacturers (including importers) of new motor vehicles and motor vehicle engines no longer have to measure, report, or comply with federal GHG emission standards. The final rule removes all GHG emission regulations in 40 CFR:

  • Parts 85, 86, and 600 (light- and medium-duty vehicles);
  • Part 1036 (heavy-duty vehicle engines); and
  • Part 1037 (heavy-duty vehicles).

The final rule also eliminates:

  • All off-cycle credits for the addition of certain technological features (e.g., high-efficiency exterior lighting, waste heat recovery, and active seat ventilation); and
  • EPA’s incentives for manufacturers to add a start-stop system (which automatically shuts off a vehicle’s engine during idling).

What doesn’t change?

EPA’s following regulations remain in effect for new motor vehicles and vehicle engines:

  • Criteria pollutant and air toxic measurement and standards,
  • Corporate Average Fuel Economy testing, and
  • Associated fuel economy labeling requirements.

About the 2009 Endangerment Finding

In 2009, EPA issued two findings: the Endangerment Finding and the Cause or Contribute Finding. Collectively, these findings are referred to as the 2009 Endangerment Finding. The agency used the 2009 Endangerment Finding as the legal basis to regulate GHG emissions from new motor vehicles and vehicle engines under Section 202(a) of the Clean Air Act.

EPA regulated GHG emissions from new motor vehicles and vehicle engines through:

  • Emission standards and related requirements, and
  • Engine and vehicle certification requirements.

However, upon reconsideration, EPA stated that it no longer believes it has the statutory authority under Section 202(a) of the Clean Air Act to regulate GHG emissions from new motor vehicles and vehicle engines. Therefore, the agency has simultaneously rescinded the 2009 Endangerment Finding and repealed the related federal GHG emission regulations.

Key to remember: EPA's final rule eliminates the 2009 Endangerment Finding and the related GHG emission requirements for on-highway vehicles and vehicle engines.

EPA delays CCR management unit reporting, related requirements
2026-02-13T06:00:00Z

EPA delays CCR management unit reporting, related requirements

The Environmental Protection Agency (EPA) issued a final rule that extends the deadlines for Facility Evaluation Reports (FERs) required for active and inactive coal combustion residuals (CCR) facilities. The final rule also delays compliance deadlines for related requirements that apply to CCR facilities with CCR management units (CCRMUs).

Who’s impacted?

The final rule applies to:

  • Active CCR facilities, and
  • Inactive CCR facilities with inactive surface impoundments (i.e., legacy CCR surface impoundments).

The 2024 Legacy Final Rule (40 CFR Part 257 Subpart D) requires active CCR facilities and legacy CCR surface impoundments to submit FER Part 1 and FER Part 2, identifying any CCRMUs of 1 ton or more on-site. CCRMUs include previously unregulated CCR surface impoundments and landfills that closed before October 19, 2015, as well as inactive CCR landfills.

Additionally, the 2024 Legacy Final Rule requires facilities with CCRMUs to:

  • Establish a website to publicize the facility’s CCR information;
  • Conduct groundwater monitoring activities (specifically, install a groundwater monitoring system, develop a sampling and analysis plan, collect independent samples, and perform detection and assessment monitoring);
  • Submit the initial annual groundwater monitoring and corrective action (GWMCA) report; and
  • Comply with closure and post-closure care obligations.

What are the changes?

EPA’s final rule extends compliance deadlines for the following standards:

Compliance requirement(s)2024 Legacy Final Rule deadline2026 final rule new deadline
Establish CCR websiteFebruary 9, 2026February 9, 2027
Submit FER Part 1February 9, 2026February 9, 2027
Submit FER Part 2February 8, 2027February 8, 2028
Install groundwater monitoring systemMay 8, 2028February 10, 2031
Develop groundwater sampling and analysis programMay 8, 2028February 10, 2031
  • Start detection and assessment monitoring
  • Start evaluating groundwater monitoring data for statistically significant increases over background levels and statistically significant levels over groundwater protection standards
May 8, 2028February 10, 2031
Submit initial GWMCA reportJanuary 31, 2029January 31, 2032
Submit closure planNovember 8, 2028August 11, 2031
Submit post-closure care planNovember 8, 2028August 11, 2031
Initiate closureMay 8, 2029February 9, 2032
Key to remember: A final rule delays the deadlines for the Facility Evaluation Reports and related requirements for active and inactive coal combustion residuals (CCR) facilities with CCR management units.
Expiring TSCA CBI claims: How to request an extension
2026-02-12T06:00:00Z

Expiring TSCA CBI claims: How to request an extension

How do businesses keep confidential information “off the record”? Companies that are required to report on federally regulated chemical substances may soon face this question, as the first round of confidential business information (CBI) claims starts expiring in June 2026.

Thankfully, the Environmental Protection Agency (EPA) has answered how to keep CBI off the record. On January 6, 2026, the agency published in the Federal Register the process to request extensions of expiring CBI claims for information submitted under the Toxic Substances Control Act (TSCA).

Here’s what you need to know.

CBI extension request process

Businesses that seek to extend a CBI claim beyond its expiration date must submit an extension request. The Federal Register notice describes the following general process:

1. EPA notifies the entity of an expiring CBI claim.

The agency will publish a list of TSCA submissions with expiring CBI claims on the Confidential Business Information Under TSCA (TSCA CBI) website at least 60 days before the claims expire.

EPA will also notify submitters directly through its online Central Data Exchange (CDX). Verify that your company’s contact information on CDX is updated!

Submitters with CBI claims for specific chemical identities should reference the TSCA Chemical Substance Inventory (column EXP) to confirm expiration dates.

2. The entity submits an extension request.

The extension request for an expiring CBI claim includes:

  • A certified supporting statement confirming the four assertions at 40 CFR 703.5(a), and
  • Answers to EPA’s substantiation questions.

EPA lists the general questions that apply to all CBI claims at 703.5(b)(3). Additional questions at 703.5(b)(4) apply to entities claiming CBI for specific chemical identities.

Businesses must submit the extension through EPA’s CDX at least 30 days before the CBI claim expires. The agency is currently developing a new application on CDX for submitting extension requests, which it plans to launch before CBI claims begin expiring in June 2026.

If there’s a delay, EPA will notify submitters on the TSCA CBI website. Additionally, the agency won’t publicize any information from expiring CBI claims until businesses have the opportunity to submit extension requests and the agency reviews them.

3. EPA reviews the extension request.

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

If the agency denies the extension request, the information in the CBI claim can be publicized once the claim expires. EPA will notify submitters of denied claims through CDX at least 30 days before it plans to disclose the information.

Expiring CBI claims: What are the options?

Regulated entities have three ways to address expiring CBI claims:

  • If you choose to maintain the CBI claim, submit the extension request to EPA.
  • If you decide not to renew the CBI claim, you can either:
    • Withdraw the CBI claim through CDX, or
    • Allow the CBI claim to expire (i.e., take no action).

Keep in mind that if you withdraw a CBI claim or allow it to expire, EPA can publicize this information without notifying you beforehand.

Who’s impacted?

The CBI extension request process applies to companies that have made CBI claims under TSCA on or after June 22, 2016.

The Frank R. Lautenberg Chemical Safety for the 21st Century Act (signed into law on June 22, 2016) made amendments to TSCA, including adding a 10-year expiration date to CBI claims.

Key to remember: EPA established the process for entities to request extensions of expiring CBI claims for information submitted under TSCA.

Common errors companies make when submitting air emissions inventories
2026-02-10T06:00:00Z

Common errors companies make when submitting air emissions inventories

Submitting accurate air emissions inventories (AEIs) is essential for regulatory compliance, public transparency, and long-term environmental planning. Yet companies routinely make mistakes that delay approvals, trigger enforcement, or compromise data quality. Many of these errors stem from misunderstanding the reporting rules, such as the Environmental Protection Agency's (EPA’s) Air Emissions Reporting Requirements (AERR) and Greenhouse Gas Reporting Program (GHGRP). Awareness of these pitfalls helps facilities avoid compliance failures and improve emission tracking systems.

Misunderstanding what must be reported

One of the most common errors is failing to understand which pollutants must be included. Under the AERR, states and delegated agencies must report annual emissions of criteria air pollutants, including sulfur dioxide, nitrogen oxides, volatile organic compounds, carbon monoxide, lead, particulate matter (PM2.5 and PM10), and ammonia. These pollutants drive national air quality planning and modeling.

However, many companies overlook hazardous air pollutants (HAPs). While past AERR rules made HAP reporting voluntary, EPA’s proposed revisions would require annual HAP reporting for many sources starting in 2027, significantly expanding reporting duties. Failing to include HAP data or assuming it's still voluntary is a growing compliance risk.

Greenhouse gases (GHGs) are another reporting blind spot. The GHGRP requires large emitters and certain suppliers to report carbon dioxide (CO2), methane, nitrous oxide, and other GHGs each year. Companies often assume GHG reporting applies only to the largest industries, yet thousands of facilities fall within the rule’s thresholds.

Using incorrect or incomplete emission calculations

Facilities often make calculation errors when converting raw activity data into emissions. Many rely on outdated emission factors or incomplete process data. EPA urges states and regulated entities to use standardized estimation guidance from the Air Emissions Inventory Improvement Program whenever possible. But companies may choose default factors without confirming they apply to the specific process, control efficiency, fuel type, or measurement method.

Under EPA’s proposed AERR revisions, if approved, the agency will require more detailed stack information, such as release point coordinates, exhaust parameters, control device data, and stack test results. Failure to collect these details early can lead to rushed estimates or missing data.

Misreporting source categories

Another major issue is misidentifying emission sources. The AERR distinguishes between point, nonpoint, mobile, and portable sources. Mislabeling a source may cause a facility to submit incomplete inventories or fail to meet the required reporting frequency. For example, point sources often require annual reporting, while nonpoint sources may follow triennial schedules.

Similarly, GHGRP reporting is broken into numerous subparts that define equipment types, fuel suppliers, industrial processes, and CO2 injection activities. Companies sometimes choose the wrong subpart or assume their process is exempt, leading to incomplete data submissions.

Incorrect use of thresholds and applicability

Both the AERR and GHGRP have emission-based thresholds. Companies frequently make errors when determining:

  • Whether they meet the AERR Type A point source criteria;
  • Whether they exceed GHGRP reporting thresholds (generally 25,000 metric tons CO2 equivalent annually); and
  • Whether HAP emissions exceed thresholds when HAP reporting is required by a state.

These mistakes usually occur when internal data systems lack consistent tracking or when actual emissions deviate from "potential to emit" estimates used in permitting.

Missing documentation and recordkeeping

EPA requires extensive documentation for emission calculations, monitoring methods, stack tests, control equipment operation, and assumptions. GHGRP rules include detailed monitoring, Quality Assurance/Quality Control (QA/QC), missing data, and record retention requirements. Under proposed AERR rules, companies would also need to submit performance test and evaluation data. Missing or incomplete records often lead to rejected inventories.

Failing to track regulatory updates

Both the AERR and GHGRP are undergoing major revisions. EPA’s proposed AERR updates aim to convert some triennial reporting to annual schedules, add HAP reporting, expand mobile source requirements, and require more detailed facility-level data. Meanwhile, the GHGRP is facing proposed cuts that would eliminate reporting requirements for many source categories while delaying petroleum and natural gas reporting until 2034.

Companies that rely on outdated guidance or assume reporting rules remain static are at risk of major compliance failures.

Improving AEI quality and compliance

Avoiding common errors begins with three fundamentals:

  • Use current regulatory guidance, emission factors, and calculation tools;
  • Maintain complete process data, stack test records, and QA/QC documentation; and
  • Assign knowledgeable staff to track AERR, GHGRP, and state-level changes.

Key to Remember: Accurate air emissions inventories play a crucial role in protecting public health, supporting air quality regulation, and demonstrating corporate responsibility. By understanding the most common pitfalls, companies can improve compliance and reduce costly reporting errors.

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