Event Detail
Practical Applications of the ICH, OECD and other relevant regulatory guidance's in Drug Development
February 11, 2010
- Palo Alto CA UNITED STATES
ComplianceOnline
Detailed review of the components of ICH, OECD and other key regulatory guidances as they relate to drug safety, quality and efficacy for global submissions. The specific data sets and timing of studies needed at each stage of drug development process will be presented and discussed.
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