Home > Uncategorized > CBER’s Direct Recall Classification Program Webinar: Materials Available

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For those unable to attend, presentation slides and an archived version of the presentation is available on the FDA Basics website.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!

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    August 29, 2013 at 4:25 pm

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  3. Bouzidi Belgacem
    September 4, 2013 at 12:33 pm

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  4. Bill
    September 23, 2013 at 11:25 pm

    Good devices and procedures serve the clients but faulty equipment place them at risk. Anything that helps identify and speed the process of recalls has value.

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    October 29, 2013 at 4:49 am

    Great Blog ! Thank you so much for topic

  6. zolahut
    November 23, 2013 at 6:52 am

    i will join for the next FDA Basics webinar! thank you so much

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    December 18, 2013 at 12:30 pm

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    December 26, 2013 at 2:11 pm

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  9. Bob
    January 26, 2014 at 6:43 am

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    May 29, 2014 at 5:01 pm

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    June 28, 2014 at 2:50 am

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  14. icici
    July 1, 2014 at 7:04 am

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  15. Nina Fire
    July 14, 2014 at 4:50 pm

    This article helped me a lot. Just opened my mind :D thanks

  16. Thomas
    October 27, 2014 at 8:45 pm

    Is there a replay available? Just discovered that post here….

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