July: CBER's Direct Recall Classification Program
DATE: July 25, 2013
TIME: 2:00pm EDT
LENGTH: 30 minutes
Do you know the vital role that FDA plays in product recalls and how the Direct Recall Classification program gets recall information to consumers in a more timely manner?
Consumers are impacted by FDA-regulated products every day. Conducting a recall is an effective way for a firm to remove or correct a violative, and possibly dangerous, product from the market. FDA advises firms on their recall strategies and monitors their recall to determine whether it is effective. FDA also publicizes recalls so consumers and health professionals can find out what types of products are being recalled.
On Thursday, July 25th, FDA hosted a webinar that explains the Direct Recall Classification (DRC) program and its importance to consumers. Laura Hieronymus, Senior Recall Coordinator with the Office of Compliance and Biologics Quality in FDA’s Center for Biologics Evaluation and Research, discussed the importance of timely recall information for consumers and the impact DRC has had on speeding up the information flow between industry and FDA.
After the presentation, there was an opportunity to ask questions.
Webinar Slides: CBER’s Direct Recall Classification Program
View an archived version of the presentation: https://collaboration.fda.gov/p24kew6aosb/
- FDA Basics Webinar - April 27, 2015: Drug Trials Snapshots
- Webinar Friday, May 23 - Packing A Healthy Lunch
- How can I share my ideas and suggestions with FDA?
- FDA Basic Video: Terry Toigo Talks About Helping Patients and their Families (Video)
- Where should I go to find consumer information on www.FDA.gov?
- Does FDA regulate dietary supplements for animals?
- Webinar: 20 Years Later – Returning to FDA to Regulate Tobacco
- Connect with Us: Using FDAs Digital Tools to Present, Participate and Personalize Tobacco Information
- FDA Center for Tobacco Products Inaugural Year and Looking Forward
- FDA Basics Metrics: February 2015
- FDA Basics Metrics: January 2015
- What are Veterinary Biologics (including vaccines) and is FDA responsible for these products?
- FDA Basics Metrics: December 2014
- FDA Basics Webinar: FDA CBER Mini-Sentinel Program
- Recall Process for FDA-Regulated Products
- FDA Basics Metrics: November 2014
- FDA Basics Webinar - November 24, 2014: Drug Shortages
- FDA's MedWatch Program: Voluntarily Reporting Problems to the FDA
- FDA Basics Webinar June 30, 2014: Over-The-Counter Medicines and Driving
- Webinar Tuesday, May 13 - Temporary Tattoos: Raising Consumer Awareness of Safety
- FDA Basics Webinar November 5, 2014: CVM’s Pet Food Reporting and Recall Process
- FDA Basics Metrics: October 2014
- FDA Basics Metrics: Septemeber 2014
- Who can I contact if my question wasn’t answered or if I have additional questions in the future?
- What Should I Do If I See Violations of FDA’s Tobacco Products Rules?
How helpful was this information?