World Conference Calendar

33622 Conferences

China - Compliance Processes for Life Science Products: Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations

Added by Referral on 2010-11-18

Conference Dates:

Start Date Start Date: 2011-02-10
Last Date Last Day: 2011-02-10

Conference Contact Info:

Contact Person Contact Person: admin
Email Email: admin@complianceonline.com
Address Address: 2600 E. Bayshore Road, Online Event,Palo Alto, CA, 94303, United States
Phone Tel: 650-620-3915
Phone Fax: 650-963-2556

Conference Description:

This China life science compliance based webinar will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations.

This 3 hrs course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in China. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in China. Content will also include descriptions of the methods by which regulators in the SFDA process filings and registrations and what is expected in the authorization and dossier maintenance of licensed products.

Who Will Benefit:

This course will be beneficial to:

Regulatory, Quality, Manufacturing, Global Business Development and General Management personnel whose responsibilities require knowledge of China’s regulatory, quality and import / export requirements
Administrative staff responsible for ensuring compliance with regulatory filings and overall GCP, GMP and GLP compliance requirements will also find this training highly relevant
Global business development and general management requiring an understanding of how regulations and compliance issues are culturally handled along with how best to consider China into one’s Global Business Strategy will profit from attending
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