Clinical Research and Product Registration of Biopharmaceuticals/Vaccines in India and China

Venue: Omni San Diego Hotel

Location: San Diego, California, United States

Event Date/Time: Apr 26, 2007 End Date/Time: Apr 27, 2007
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The conference aims to provide a detailed analysis of what it takes to conduct clinical trials from a biopharmaceuticals and vaccines perspective in India and China, to address: risk/benefit balance; anecdotal experiences of the multinational pharmaceutical industry in China and India; selection and role of CROs; logistics of operations; clinical trials management; government policies (including IPR issues); and pharmacovigilance.

Keynote Address:
Why India and China – Emerging Markets in Biopharmaceutical Development

•Why India and China – Emerging Markets in Drug Development and Conducting Clinical Research in India and China: New and Experienced Perspectives.
•Logistics and Operations of Clinical Research in China and India for Biopharmaceuticals
•Strategic Outsourcing and Partnership with China and India – CRO Infrastructure, Analysis and Performance
•Drug Registration of Biopharmaceuticals/Vaccines in China and India – (Process of drug registrations)
•Government Policy and Regulatory Environment
•Trade-related Aspects of Intellectual Property Rights (TRIPS) and Government Policies in Both China and India
•Data Management: China and India
•Early Phase and Phase I Clinical Trial Conduct: China and India.


675 L Street
San Diego
United States