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.
Process Validation for Medical Device Manufacturers
22 April 2011, Palo Alto, United States
Introduction
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
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
650-620-3915
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