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CD-Navigating the FDA's Reportable Food Registry (Webinar Series)
Price: $500.00 | Mbr Price: $250.00
Item Code: CDRFR
Recently the Food and Drug Administration (FDA) implemented the long-awaited Reportable Food Registry (RFR), created by an amendment to the Federal Food, Drug and Cosmetic Act (FFDCA). The RFR is an electronic portal by which instances of reportable food(s) must be submitted to FDA, according to the FFDCA amendment. After receipt of reports through the portal, FDA is required to review and assess the information submitted for purposes of identifying reportable foods, issuing an alert or notification, or exercising other actions to protect the public health.
In this latest installment of the GMA Webinar Series Navigating the FDA's Reportable Food Registry: Parsing the Portal, December 17, 1:00-2:30 p.m. EST, GMA science and regulatory experts covered new and updated information that will help CPG companies navigate the nuances of this new tool. Topics covered included:
- Is there an FDA period of "regulatory discretion"?
- Common portal problems and how to avoid them
- What is being reported that doesn't need to be?
- Common key reporting omissions
- The most problematic reporting challenges
- New issues in amending existing RFR reports
- Anticipated portal enhancements
- Recordkeeping requirements for those reporting, subsequent receipients, and immediate poast source providers
- Safety Report Disclaimers and the RFR
- Disclosure of RFR reporting information
Duration: 1.5 Hours |
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