This webinar will help clinical laboratories, analyzing samples from clinical trials, understand the compliance requirements concerning ICH GCP for FDA and EMA (new requirements 2012) compliance.
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
14 September 2013, Palo Alto, United States
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ComplianceOnline
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Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States
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