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2026-07-02T05:00:00Z
NewsIndustry NewsIndustry NewsFleet SafetyCMV Parts and MaintenanceVehicle TechnologyVehicle TechnologyFleet OperationsFocus AreaEnglishBrakesTransportationUSA
Commonsense update to AV brake pedal requirements
The National Highway Traffic Safety Administration (NHTSA) recently removed the mandate for manual brake pedals in autonomous vehicles (AVs) as part of its efforts toward “commonsense” measures. This applies to vehicles designed to be driven exclusively by automated driving systems with no human behind the wheel.
This action is the fifth update to the DOT’s Federal Motor Vehicle Safety Standards (FMVSS), aligning with previous actions to remove the types of equipment vehicles won’t need if a human being is not present in the vehicle (e.g., windshield wipers, rearview mirrors, etc.).
NHTSA says it will continue enforcing all other brake-related requirements, such as stopping distance standards.
Along with removing brake pedals, NHTSA has also made the following FMVSS updates:
- Assured its further development of real-world safety performance for AVs,
- Removed requirements for hand- or foot-operated brake controls for vehicles that won’t be driven by a human,
- Declared that all subject vehicles must still meet the expected stopping distance performance criteria, and
- Stated its continued authority to oversee recalls investigate unsafe automated driving behaviors.
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2026-07-02T05:00:00Z
NewsIndustry NewsHR GeneralistFamily and Medical Leave Act (FMLA)In-Depth ArticleFamily and Medical Leave Act (FMLA)HR ManagementEnglishUSAFocus AreaHuman Resources
Must employers accept FMLA certifications from online services?
Under the federal Family and Medical Leave Act (FMLA), in-person treatment for a serious health condition can include an appointment with a health care provider via telemedicine (i.e., a virtual visit), as long as it involves video.
The law doesn’t specify where the health care provider must be. Employees may, therefore, obtain an FMLA certification from online health care providers through a service dedicated to completing FMLA certifications.
Some services boast that they have licensed health care providers on staff who review an individual’s “case” and complete an FMLA certification within 24 hours. Others work with independent doctors. The review includes a video visit, so it meets the FMLA’s “telemedicine” requirement.
Such providers charge for the service, from $49 to $149, depending on the service and speed. Some claim that, if the employer doesn’t accept the certification, the employee gets their money back.
Employees are responsible
When employers ask employees to obtain a certification to support the need for FMLA leave, employees are responsible for complying. Employees might, however, find it hard to get an appointment to see their own health care providers. If they don’t have a primary care physician, they might need to become an established patient before even being seen.
This can all take time. Employees have 15 calendar days to obtain a certification unless extenuating circumstances are involved. Getting an appointment with a new provider might take more than 15 days. Even if an employee or family member is an established patient, they might not be able to get an appointment within 15 days.
Therefore, online services might be a viable and less expensive option for employees, as they can get same-day appointments in certain situations.
Employers are responsible
Employers might not know where a health care provider is or what entity they work for. As long as the health care provider is authorized to practice medicine or surgery (as appropriate) by the state in which they practice, employers should accept a complete and sufficient certification. The health care provider doesn’t have to be in the same state as the employee (or family member).
Employers shouldn’t dictate the particular health care provider from whom an employee obtains a certification, but can guide employees to alternative options as needed.
Key to remember: Employers should accept FMLA certifications from online service providers, as long as the certifications are otherwise complete, sufficient, and signed by a licensed health care provider.
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2026-07-02T05:00:00Z
NewsIndustry NewsFleet SafetyDriver qualificationsDrivers qualification (DQ file)Driving RecordsDriver abstractsAnnual MVR reviewFocus AreaIn-Depth ArticleEnglishTransportationUSA
Common motor vehicle report (MVR) questions and misconceptions
Motor vehicle reports (MVRs) are one of the most valuable tools for evaluating driver qualification, identifying risky driving behaviors, and reducing liability exposure.
Whether you're managing commercial driver’s license (CDL) drivers, non-CDL drivers, or employees who occasionally operate company vehicles, understanding MVR requirements can help you make better hiring, qualification, and safety decisions.
Who needs an MVR?
Some employers may think MVR requirements only apply to CDL drivers, but that's not the case. Any employee operating commercial motor vehicles (CMVs) that meet the federal definition of a CMV is subject to driver qualification requirements regardless of whether they hold a CDL.
This can include non-CDL drivers, supervisors, mechanics, owners, or other employees who occasionally operate regulated vehicles. If a person drives a CMV in interstate commerce, they must meet the same qualification standards as a full-time driver.
When should the initial MVR be obtained?
For non-CDL drivers subject to the driver qualification regulations under 391.51, employers must obtain the MVR within 30 days of hire. As a best practice, however, many fleets review an MVR before allowing a driver behind the wheel.
For CDL drivers, the MVR serves an additional purpose. It’s also used to verify DOT medical certification status and must be obtained before allowing a driver to operate a CMV.
How often should MVRs be reviewed?
Regulations require motor carriers to obtain and review a driver’s MVR at least once every 12 months. The review should evaluate licensing status, convictions, restrictions, endorsements, and any other changes that could affect the driver's qualifications. Drivers should also be reviewed against your internal policies on established safe driving thresholds — or as it’s often referred to, your “points” or “scoring” system.
An annual MVR is the minimum requirement, and a lot can change on a driver’s record if you’re waiting a full year to run their MVR. Many fleets have moved beyond annual reviews and now use continuous MVR monitoring programs, or run more frequent MVRs, such as quarterly reviews. This practice is highly recommended and will help carriers avoid being blindsided by a disqualified driver.
3 MVR misconceptions
Misconception #1: A valid license means the driver is low risk.
A driver may still hold a valid license while accumulating speeding convictions, distracted driving violations, preventable crashes, or other indicators of elevated crash risk. Looking only at license status or disqualifications can cause carrirs to miss driving patterns that warrant coaching or corrective action.
Carriers should include an internal “scoring” system in their company policies to consistently evaluate drivers and set clear expectations.
Misconception #2: Drivers will tell us when something changes.
CDL drivers must report traffic convictions, and all CMV drivers are required to report certain losses of driving privileges. However, relying solely on self-reporting leaves carriers vulnerable to delays, misunderstandings, and missed notifications.
Misconception #3: MVRs are simply a compliance document.
The most successful carriers use MVRs to support safety management programs. A speeding conviction, failure-to-yield violation, or pattern of unsafe driving behaviors can become an opportunity for coaching and training before a crash occurs.
Make sure whoever reviews MVRs is trained and knows exactly what to look for, and ask questions when warranted. Missing something because it wasn’t clear on the MVR isn’t a valid excuse.
What should carriers do when an MVR reveals a problem?
The answer depends on the severity of the issue and company policy. In some situations, coaching or refresher training is appropriate. In others, progressive discipline or removal from driving duties may be necessary. This may also involve working with your HR department to ensure appropriate steps are taken.
The key is consistency. Carriers should establish written policies, communicate expectations to drivers, and apply corrective actions consistently when your standards aren’t met.
Key to remember: An MVR is more than a simple check-the-box compliance item. It provides key insight into driving habits, qualification status, and potential safety risks. Organizations that proactively review and act on MVR information are better positioned to prevent crashes, reduce liability, and demonstrate strong safety management practices.
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2026-07-01T05:00:00Z
NewsHR ManagementEnglishHuman ResourcesTalent Management & RecruitingAssociate Benefits & CompensationIndustry NewsIndustry NewsDiscriminationTitle VII (The Civil Rights Act of 1964)Affirmative ActionRecruiting and hiringRecruiting and hiringHR GeneralistEEO-1 ReportingAssociate RelationsFocus AreaUSA
EEOC rescinds guidance on voluntary affirmative action plans
On June 30, the U.S. Equal Employment Opportunity Commission (EEOC) announced that it had voted to rescind two documents relating to permissible affirmative action under Title VII of the U.S. Civil Rights Act.
The two documents that were rescinded include the agency’s:
- 1979 regulatory guidelines on “appropriate” affirmative action under the statute; and
- Section 607 of its Compliance Manual, which addressed those guidelines and the agency’s enforcement positions with respect to permissible affirmative action and affirmative action plans.
Rescission of the EEOC’s guidance doesn’t, however, reverse the Supreme Court’s decisions in United Steelworkers v. Weber, 443 U.S. 193 (1979) and Johnson v. Transportation Agency, 480 U.S. 616 (1987), in which the Court recognized that Title VII may allow for certain voluntary affirmative action plans in limited circumstances.
Part of broader changes
The EEOC’s proposal is in line with other previous and pending changes affecting affirmative action and workforce reporting requirements. For example, federal contractor obligations to maintain affirmative action plans under regulations administered by the Department of Labor's Office of Federal Contract Compliance Programs were eliminated in 2025 after the president rescinded the executive order that established them.
The EEOC is also pursuing the rescission of EEO-1 data collection and reporting rules which require companies and public employers to report workforce demographic information, including data on race, sex, and national origin.
What should employers do now?
In lieu of the EEOC’s actions, employers may want to assess whether any existing policies or programs could be affected by changes in the federal government’s approach to affirmative action.
Key to remember: The EEOC has guidance for employers that voluntarily maintain affirmative action plans.
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2026-07-01T05:00:00Z
NewsWage and Hour Division (WHD), DOLIndustry NewsIndustry NewsHR GeneralistFamily and Medical Leave Act (FMLA)Family and Medical Leave Act (FMLA)USAHR ManagementEnglishFocus AreaHuman Resources
The FMLA and treatment outside the U.S.
While hiking on vacation in the Andes, Veronica fell and injured her ankle. She saw a local doctor who prescribed her pain medication, and she was laid up for 5 days. When she returned to work the following week, she told Glen, her supervisor, about the incident. Glen wondered if he had to do anything in relation to the incident, and whether the situation could involve leave under the federal Family and Medical Leave Act (FMLA).
Glen then thought about other related situations, such as:
- When employees need to care for a family member who lives outside the U.S.
- When employees visit family members in other countries, and a family member develops a medical condition.
- When employees decide to get treatment for their medical condition from a health care provider in another country.
Glen was right to be curious, as employees may take FMLA leave for their own condition or that of a family member, even if they receive medical treatment outside the U.S.
What the FMLA regulations say
The regulations cover situations involving treatment outside the U.S. They say:
In circumstances in which the employee or a family member is visiting in another country, or a family member resides in another country, and a serious health condition develops, the employer shall accept a medical certification as well as second and third opinions from a health care provider who practices in that country. Where a certification by a foreign health care provider is in a language other than English, the employee must provide the employer with a written translation of the certification upon request.
Reference: 29 CFR 825.307(f)
While this focuses on getting an FMLA certification from health care providers outside the U.S, employers have to count leave supported by a foreign certification as FMLA leave.
Employers also might wonder if employees may take FMLA leave to voluntarily obtain treatment outside the U.S, since the regulation doesn’t specifically address this. According to a representative from the U.S. Department of Labor’s Wage and Hour Division (WHD), yes, they may.
FMLA health care providers can be beyond the U.S. borders, whether they provide treatment to employees or their family members with serious health conditions. Employers should count such time off as FMLA leave.
Travel time
The WHD recently indicated that eligible employees may use FMLA leave to travel to or from a medical appointment, even if a certification doesn’t indicate the need for, time required, or other particulars of such travel time.
Key to remember: Employees may take FMLA leave to care for a family member in another country, or when they receive treatment for their own condition in another country.
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2026-07-01T05:00:00Z
NewsIndustry NewsIndustry NewsPesticidesPesticide Registration and LabelingEnvironmental Protection Agency (EPA)EnvironmentalEnglishFocus AreaPesticidesUSA
EPA sets MyPeST compliance reporting deadlines for bilingual pesticide labeling requirements
The Environmental Protection Agency (EPA) published instructions and deadlines for pesticide registrants to report compliance with bilingual labeling requirements in the MyPeST application. The first compliance reporting deadline is July 31, 2026, for pesticide products with the highest toxicity.
Who’s impacted?
Compliance reporting applies to registrants of pesticide products subject to the bilingual labeling requirements established by the Pesticide Registration Improvement Act of 2022 (PRIA 5) amendments to the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA).
PRIA 5 requires all end-use pesticide product labels to provide Spanish translations of the human health and safety sections by including the translated sections directly on the label or providing a link via scannable technology or other readily accessible electronic methods to the translated sections. EPA allows certain antimicrobial and non-agricultural pesticide products to comply by providing access to Spanish-language Safety Data Sheets instead of direct label translations.
Compliance timelines are based on the type of pesticide and its toxicity category.
What’s required?
Pesticide registrants must report compliance with the PRIA 5 bilingual labeling requirements using EPA’s MyPeST app. The agency recently published detailed reporting instructions in the MyPeST Application User Guide (accessible in the MyPeST app).
EPA also established the following deadlines for reporting compliance in MyPeST:
| Pesticide product type | Bilingual labeling deadline | Compliance reporting deadline |
|---|---|---|
| Restricted use pesticides (RUPs) | December 29, 2025 | July 31, 2026 |
| Non-RUP agricultural products | ||
| Acute Toxicity Category I | December 29, 2025 | July 31, 2026 |
| Acute Toxicity Category II | December 29, 2027 | January 28, 2028 |
| Antimicrobials and non-agricultural products | ||
| Acute Toxicity Category I | December 29, 2026 | January 28, 2027 |
| Acute Toxicity Category II | December 29, 2028 | January 28, 2029 |
| All other pesticide products | December 29, 2030 | January 28, 2031 |
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