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FDA Design Dossier: DHF, DMR, and DHR Requirements for Medical Devices

Webinar on FDA's Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) will examine existing and proposed requirements for the U.S. FDA's DHF per the Current Good Manufacturing Practices (CGMPs), 21 CFR 820.30 (j).

https://www.complianceglobal.us/product/700098

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Goldshaw Greenblatt Pierce LLC

Experienced Philadelphia employment, criminal defense & civil rights lawyers. Goldshaw Greenblatt Pierce delivers skilled advocacy for clients throughout the region.

ggplawfirm.com · Legal Consulting · 7 months remaining · Details

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