This course will present, in one place, the regulations and guidelines that apply to early phase products. In some cases these will not be regulations, but needs that, if met, will increase the efficiency of activities as a product proceeds through the development process. The course will present these items in the order of product development from the point of R & D activities to the completion of Phase 2 clinical trials.
RAPS Approved Seminar on GMP and Regulatory Expectations for Early IND Products At Mumbai
18 - 20 June 2012, Mumbai, India
Introduction
Venue
Intercontinental The LaLit
Intercontinental The LaLit, Sahar Airport Road, Maharastra, Andheri East, Mumbai, 400069, India
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GlobalCompliancePanel
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