Foundation for FDA

Trusted

http://www.reaganudall.org/

Last activity: 14.10.2026

Active

Categories: DevelopmentDrugFoodTechITNonprofitProductPublicScienceTechnologyWebsite

What better way to say nonpartisan than for Congress to name us after Ronald Reagan and Mo Udall? Back in 2007 the call to action was to identify, fund, and support projects and programs that help equip FDA staff with the highest caliber science and technology. We're on it. And you can join us.

For example, you can share our newly launched expanded access Navigator website with patients and physicians researching the complexities of compassionate use. Or if you're a company, list your expanded access policies on the Navigator's Directory or check out our IMEDS public-private partnerships.

Other ways to help us help FDA include donations to our Fellowship program or joining us at the first-ever "Innovations in Regulatory Science" Gala. It's all on our site www.reaganudall.org.

Twitter Facebook LinkedIn Youtube Email

Likes

Followers

925

Followers

2.57K

Website visits

14.4K /mo.

Mentions

Overview

Location

United States, Washington

Employees

1-10

Phone

+1 202-849-2075

Founded date

2007

Mentions in press and media 24

Date	Title	Description
Sign up to see	Sign up to see	Sign up to see
Nov 1, 2025	FDA Acts to Protect Children from Unapproved Fluoride Drug Products	For Immediate Release: October 31, 2025 The U.S. Food and Drug Administration today announced actions to restrict the sale of unapproved ingestible fluoride prescription drug products for children. The FDA sent notices to four companies out...
Oct 31, 2025	FDA Acts to Protect Children from Unapproved Fluoride Drug Products	For Immediate Release: October 31, 2025 The U.S. Food and Drug Administration today announced actions to restrict the sale of unapproved ingestible fluoride prescription drug products for children. The FDA sent notices to four companies out...
Oct 31, 2025	Ingestible Fluoride Drug Products	FDA recommends that ingestible fluoride drug products be limited to children aged three years and older who are at high risk for tooth decay. Read FDA's assessment of the benefit/risk considerations regarding the use of ingestible fluoride ...
Dec 26, 2024	FDA recommends changes to labeling for transmucosal buprenorphine products indicated to treat opioid use disorder	Today, FDA issued the Federal Register notice, Modifications to Labeling Buprenorphine-Containing Transmucosal Products for the Treatment of Opioid Dependence, to encourage the submission of supplemental new drug applications to modify the ...
Sep 24, 2024	Confusion persists with food traceability rule as compliance date nears	Listen to the article 5 min This audio is auto-generated. Please let us know if you have feedback. In a little over a year, grocers and their suppliers will need to comply with the Food and Drug Administration’s new food traceability requir...
Sep 9, 2024	The FDA's Evolving Role in Public Health and Innovative Research	The U.S. Food and Drug Administration (FDA) is a guardian of public health. It ensures the safety and efficacy of drugs, food, and medical devices. Recently, the agency has been busy, addressing a range of issues from medical device sterili...
Sep 6, 2024	FDA Roundup: September 6, 2024	SILVER SPRING, Md., Sept. 6, 2024 /PRNewswire/ -- Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: On Sept. 11 from 1-2 p.m. ET, the FDA will host a virtual Medical Device Ster...
May 22, 2024	FDA Roundup: May 21, 2024	For Immediate Release: May 21, 2024 Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA announced that registration is open for the two-day virtual public meeting, ...
Jan 22, 2024	FDA sets aggressive deadline for inspection overhaul	WASHINGTON — Food and Drug Administration officials hope to finish this year a massive overhaul of the way the agency inspects facilities that make drugs, medical devices, and food products, they said Friday. The reorganization was spurred ...
Dec 15, 2023	Health \| States strive to get opioid overdose drug to more people	Anna Claire Vollers \| (TNS) Stateline.org Posing as shoppers, a team of researchers from the University of Mississippi called nearly 600 pharmacies across the state and asked a simple, yes-or-no question: “Do you have naloxone that I can pi...
Jul 12, 2023	Real-World Evidence (RWE) Resources	Public Webinar: Considerations for the Design and Conduct of Externally Controlled Drug and Biological Products 4/24/2023 Guidance, Regulatory Considerations A Framework for Regulatory Use of Real-World Evidence Workshop 9/17/2017 Guidance,...
Apr 10, 2023	Considerations for Buprenorphine Initiation and Maintenance Care - 05/10/2023	On This Page Date: May 10 - 11, 2023 Day1: Wed, May 10 1:00 PM - 4:45 PM ET Day2: Thu, May 11 1:00 PM - 4:30 PM ET Attend the workshop: Registration through Reagan-Udall Foundation The U.S. Food and Drug Administration (FDA), in partnership...
Feb 28, 2023	FDA Provides Update on Proposed Human Foods Program and Office of Regulatory Affairs Restructuring	For Immediate Release: February 28, 2023 Today, the U.S. Food and Drug Administration announced that it has begun a national search for a new Deputy Commissioner for Human Foods and is providing an update on last month’s proposed restructur...
Feb 24, 2023	FDA Outlines Steps to Strengthen Tobacco Program	For Immediate Release: February 24, 2023 Statement From: Robert M. Califf, M.D., MACC Commissioner of Food and Drugs - Food and Drug Administration Today, the U.S. Food and Drug Administration’s Center for Tobacco Products (CTP) outlined th...
Feb 1, 2023	FDA will streamline food safety and regulation under a single leader	Dive Brief: FDA will restructure its Human Foods program, consolidating all functions and employees under a new deputy commissioner. This will bring the Center for Food Safety and Applied Nutrition, the Office of Food Policy and Response an...
Jan 26, 2023	FDA food safety chief Frank Yiannas resigns	Dive Brief: FDA Deputy Commissioner for Food Policy and Response Frank Yiannas has resigned from the position, effective Feb. 24. The resignation letter, of which Food Dive recieved a copy, is dated Wednesday. In his resignation letter, Yia...
Dec 21, 2022	Women’s Foundation for the State of Arizona Receives $350K from The Bob & Renee Parsons Foundation to Support Single Moms	Women’s Foundation for the State of Arizona “We don’t want mothers to have to choose between putting food on the table and childcare,” said Bob Parsons, Co-founder, The Bob & Renee Parsons Foundation. “Pathways for Single Moms is giving...
Dec 19, 2022	Soup-To-Nuts Podcast: What does FDA’s commitment to ‘building a world-class human foods program’ mean for industry?	FDA Commissioner of Food and Drugs Robert Califf was quick admit that the agency’s food program in recent years “has been stressed by the increasing diversity and complexity of the nation’s food systems and supply chain, the ongoing impacts...
Dec 7, 2022	FDA needs to restructure Human Foods Program, report says	Dive Brief: The FDA should restructure its Human Foods Program by providing a clear chain of command and governance model to do a more effective job of regulating food to protect public health, according to a report from the Reagan-Udall Fo...
Oct 1, 2022	FDA Continues Important Work on Substance Use and Overdose Prevention Efforts	Image By: Robert M. Califf, M.D., Commissioner of Food and Drugs Overdose prevention, reduction in opioid and other substance use disorders (SUD), and effective treatment and support for those with SUD are key priorities for the U.S. Food a...
Aug 2, 2017	New online navigator helps patients and doctors access experimental treatments	When approved therapies don’t work, or stop working, for people with serious or life-threatening illnesses, it puts them in a difficult position. Some turn to clinical trials that are testing experimental treatments. But many can’t do that ...
Apr 22, 2015	FDA to award $1M EHR mining grant for drug-safety surveillance	The Food and Drug Administration is making as much as $1 million in grant funding available for mining a large database of electronic health records to conduct postmarket surveillance of drug safety. The FDA’s Center for Drug Evaluation and...
	FDA to award $1M EHR mining grant for drug-safety surveillance	The Food and Drug Administration is making as much as $1 million in grant funding available for mining a large database of electronic health records to conduct postmarket surveillance of drug safety. The FDA’s Center for Drug Evaluation and...

Reviews 0

FAQ about Foundation for FDA

When was Foundation for FDA founded?

Foundation for FDA was founded in 2007.

What has the press written about Foundation for FDA?

Parsers VC has collected 24 articles mentioning Foundation for FDA, among them “FDA Acts to Protect Children from Unapproved Fluoride Drug Products” (Nov 1, 2025) and “FDA Acts to Protect Children from Unapproved Fluoride Drug Products” (Oct 31, 2025).

Is Foundation for FDA still active?

Yes, Foundation for FDA is active; its latest activity on Parsers VC dates from Oct 14, 2026.