HHS regulations

National Institute of Dental & Craniofacial Research announces an upcoming meeting of its advisory council to review research grant applications and program policies.

CMS is seeking public comment for 60 days on proposed information collection activities under the Paperwork Reduction Act of 1995.

FDA issues draft guidance on compliance policies for NIOSH-approved air-purifying respirators including N95s, PAPRs, and reusable respirators to streamline premarket requirements and reduce regulatory burden.

FDA draft guidance establishes impurity specifications for fermentation and semi-synthesis antibiotics in NDAs, ANDAs, and OTC monograph drugs to ensure consistent quality standards.

CMS requests public comment under the Paperwork Reduction Act on proposed information collection activities; submit comments by the deadline specified in the Federal Register notice.

HRSA's Information Collection Request for the Rural Health Network Development Planning Program measurement system is under OMB review with a 30-day public comment period required before approval.

The FDA will hold a public meeting to solicit comments on the Animal Generic Drug User Fee Act program and recommendations for its next reauthorization.

Federal agencies request public comment on proposed information collection activities that affect small businesses; submit feedback by the specified deadline to reduce regulatory burden.

ACF's Personal Responsibility Education Program Performance Measures project (OMB #0970-0497) requests continuing data collection from PREP grant recipients through revised participant surveys and reporting forms; OMB approval expires July 31, 2026.

FDA is accepting public comments for 60 days on a proposed information collection for qualitative social and behavioral research data submissions related to food, dietary supplements, cosmetics, and animal feed.

FDA seeks 60-day public comment on proposed information collection requirements for Radioactive Drug Research Committees governing radioactive drug use in basic research under the Paperwork Reduction Act.

FDA issues four Emergency Use Authorizations for animal drugs to prevent and treat New World screwworm infestations in cattle, dogs, cats, horses, and other species following HHS's August 18, 2025 public health emergency declaration.

FDA holds a virtual public meeting to solicit comments on the Animal Drug User Fee Act program and considerations for its next reauthorization.

Centers for Medicare and Medicaid Services seeks public comment on generic information collections for Medicaid and CHIP state plan amendments, waivers, demonstrations, and reporting under expedited Paperwork Reduction Act clearance.

SAMHSA proposes new information collection requirements for substance abuse and mental health services programs; public comment period details available in Federal Register notice.