CBER’s Direct Recall Classification Program Webinar: Materials Available
Thank you to all who were able to participate in FDA’s July 25th webinar that explained 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.
For those unable to attend, presentation slides and an archived version of the presentation is available on the FDA Basics website.
Thank you again and we hope you are able to join us for the next FDA Basics webinar!