💰HHS Agency Information Collection Request for Public Comment
In compliance with the requirement of the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed collection for public comment.
Learn More📄Request for Information on HHS Deregulatory Initiatives
To implement the President's Deregulatory Initiatives, including Department of Government Efficiency Deregulatory Agenda, and to better promote the health and well-being of the American people, the U.S. Department of Health and Human Services (HHS) is planning the largest deregulatory effort in the history of the Department. To facilitate this effort, HHS seeks input from all interested parties on how to dramatically deregulate across all areas the Department touches. HHS also welcomes other submissions explaining how regulations, guidance, paperwork requirements, and other regulatory obligations can be repealed.
Learn More🏥Proposed Information Collection for Family Planning Program
In compliance with the requirement of the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, is publishing the following summary of a proposed collection for public comment.
Learn More🧠Notice of Closed Meeting for Mental Health Grant Applications
The Department of Health and Human Services announces a closed meeting of the National Institute of Mental Health Special Emphasis Panel to review grant applications. This virtual event will review confidential discussions involving potential funding opportunities and evaluations related to mental health research.
Learn More🧬NIH Meetings Notice
The National Institutes of Health (NIH) announces closed meetings for various committees to review grant applications focusing on neuroscience and biomedical research. These virtual meetings will involve the evaluation of applications potentially impacting funding opportunities for businesses and research institutions engaged in scientific advancements.
Learn More💼Notice of Fogarty International Center Advisory Board Meeting
The Fogarty International Center Advisory Board will convene to review grant applications and discuss future initiatives on June 2-3, 2025. The meeting includes opportunities for public attendance, both in-person and virtually, and will cover critical updates on international health programs. Special accommodations are available for participants needing assistance.
Learn More💊FDA Notices Regulatory Review Period for JAYPIRCA Patent Extension
The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for JAYPIRCA and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Director of the U.S. Patent and Trademark Office (USPTO), Department of Commerce, for the extension of a patent which claims that human drug product.
Learn More🏥Amended Notice of Meeting - NIH Center for Scientific Review
The Department of Health and Human Services announces a change in the scheduling of a meeting for the Center for Scientific Review Special Emphasis Panel regarding health disparities technology development. The meeting will be closed to the public and features a newly assigned Scientific Review Officer.
Learn More💼NIH Closed Meetings for Grant Applications Overview
The National Institutes of Health announces closed meetings for review and evaluation of grant applications related to various health research topics. These meetings cover different committees focusing on biomedical imaging, psychosocial development, infectious diseases, and more. The discussions will remain confidential to protect trade secrets and personal privacy associated with grant submissions.
Learn More📋FDA Seeks Comments on Medical Device Reporting Regulations
The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed revision of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collections associated with requirements for medical device reporting for user facilities, manufacturers, importers, and distributors of medical devices.
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