From January 2024 to July 2024, the Federation of American Scientists interviewed 30 current and former FDA Advisory Committee (AdComm) members to learn about the Advisory Committee experience and identify existing challenges and opportunities to help inform actionable policy solutions. The goal of this project was to create a vision for how the FDA and other federal agencies can better engage external scientific experts and the public to address critical challenges facing public health. Discussions included topics such as how the FDA can better leverage Advisory Committee membership through expanding the role of the chair, overall committee composition, implementing mandatory training programs, streamlining the conflict of interest process, and more.
Based on these discussions, we were able to source potential policy recommendations that may assist with enhancing the FDA’s ability to obtain valuable advice for evidence-based decision-making. The results of these discussions are presented in case studies detailing the recurring themes that emerged and policy recommendations for improvement.
FACA Toolkit
Final Report
Protecting the health and safety of the American public and ensuring that the public has the opportunity to participate in the federal decision-making process is crucial. As currently organized, FACs are not equipped to provide the best evidence-based advice.
These recommendations can catapult the Advisory Committee structure into one that continues providing the government with the best advice.
Improving public awareness of FDA Advisory Committees would improve public trust and deter misinformation related to the approval of medical products.
The absence of consistent voting privileges for patient representatives on Advisory Committees hinders representatives from providing an voice on behalf of the community they represent.
When a hurricane hits, it’s all hands on deck – that goes for federal data, too. Pulling back from our investments in timely, accurate, and accessible public data will only make us less prepared and put us all at greater risk.
This is bigger than a singular elimination of race and ethnicity questions. It could accelerate the second wave of widespread reductions to demographic data, leaving public health officials with even less information to deliver better health outcomes for all Americans.
After a year-long delay, this April, EPA released the latest air toxics data, which only included raw air data downloads. This year, for the first time in nearly 25 years, the air toxics data did not include cancer risk estimates.
As federal data policy nerds, the question we get asked all the time is “How much data has the current administration terminated?”