#40: Understanding and Navigating the Regulatory System in China
This tutorial is designed for professionals involved in regulatory affairs, clinical research, pharmacovigilance/drug safety, project management, R&D strategies, and quality assurance and quality control.
Day & Time:June 24, 9:00AM - 5:00PM, Philadelphia, PA
This tutorial will provide an overview of the regulatory system in China, including the agencies and institutions at the central government and provincial levels, as well as their roles and responsibilities. Various regulations for product registration, clinical trials, and safety reporting will be presented, and the regulatory pathways and strategic considerations for clinical trial and marketing applications will be discussed. A step-by-step roadmap of how to navigate the regulatory system in China for clinical trial approval and product registration will also be discussed. This discussion will include key points to consider, strategies, and tactics.
for special offers and more details, http://www.diahome.org/en/flagship-meetings/dia2012/Meeting-Program/About-our-Offerings/Find-Sessions-and-Presentations/Event%20Details.aspx?productID=28310&eventType=TUTORIAL&title=#40: Understanding and Navigating the Regulatory System in China
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