This presentation will help with preparing better for submitting data obtained from outside US countries to the FDA and from US to outside FDA regulated countries. All these are done with the primary goal in mind: lowering companies' costs and speeding data transfer for quicker regulatory submission and approval.
Webinar On Differences between ICH-GCP and FDA regulations
10 March 2011, Palo Alto, United States
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Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
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ComplianceOnline
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