Medical Device Process Validation - Statistical Considerations

8 February 2012, Palo Alto, United States


Introduction
This Process Validation training will look at the underlying statistical concepts to perform an effective process validation. The webinar examine elements of the FDA regulations for process validation (21 CFR §820.75) as well as the corresponding requirements in ISO 13485.
Venue
Online Event

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

Organised by
ComplianceOnline
Contact information
Mr Referral
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email

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