|
Home
>
Newsletters
>
Drug GMP Report
> Biological Deviation Reports May Spur ‘Direct’ Recall: CBER Officials
Drug GMP Report
September 2012
Biological Deviation Reports May Spur ‘Direct’ Recall: CBER Officials
TAMPA, Fla. — Now that CBER’s all-electronic Direct Recall Classification (DRC) program has been extended to non-blood products, problems with biologic drugs flagged in electronic biological product deviation reports (eBPDRs) may trigger recalls of those products under the program.
|
|
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnews
All rights reserved. Do not duplicate or redistribute in any form.