Introduction

The FDA QSR requires device manufacturers to validate processes when the manufacturer cannot "fully verify the output". The manufacturer must validate these processes with a "high degree of assurance".

Venue

online training webinar

online training webinar, 1000 N West Street, Suite 1200, Wilmington,DE, 19801, United States

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• Venue information More information about the venue

Organised by

globalcompliancepanel

Contact information

Mr webinar web
1000 N West Street, Suite 1200, 1000 N West Street Suite,, Wilmington, United States of America
8004479407
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