The FDA on Friday, Sept. 29, will hold a public meeting titled “Modernizing Food and Drug Administration Recalls Listening Session.” Its purpose is to provide an opportunity for stakeholders, industry and the public to share information and feedback about topics related to recall modernization for FDA-regulated products.
Perceived topics are:
- General recall preparations/contingency planning
- Creating successful recall strategies, including methods to reach underserved communities
- Initiating a recall
- Strategies for public warning, including press releases, social media, and other communication tools
- Increasing efficiency and effectiveness of recall information exchange
- Ensuring effective recalls
- Terminating a recall
- Strategies for reducing recall recurrence for similar situations
It will be held in person at FDA’s White Oak Campus in Silver Spring, Md., 9am-5pm ET. It also will be webcast, details of which are shared when you register.
Registration is required, and there is a series of deadlines: Sept. 1 to attend in-person and/or to speak; Sept. 15 to email-in accompanying presentation materials; Sept. 29 to attend virtually; and Oct. 27 to submit after-the-fact written comments to the docket FDA-2023-N-2393.
Read more and register here.
