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Process Validation for Medical Device Manufacturers

22 April 2011, Palo Alto, United States


Introduction
This Process validation training/webinar for medical device manufacturers will discuss the CDRH interpretation of the GHTF guidance and how manufacturers should develop Process Validation Plans and conduct production Process Validation.

Useful links

Venue
Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

Organised by
ComplianceOnline
Contact information
Mr Ryan
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
650-620-3915

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