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.
Medical Device Process Validation - Statistical Considerations
8 February 2012, Palo Alto, United States
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Online Event
Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
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ComplianceOnline
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