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China Update: Regulatory Changes and Implications

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Continuing Education credits are not available for the archived offering.
This archived webinar is available for purchase through November 27, 2014.
Broadcast time: 1 hour 29 minutes

Recently, the China Food and Drug Administration (CFDA) has implemented or proposed several important changes in its regulations concerning drug registration, clinical trials and other areas.  There have also been changes in the regulatory review practice in areas such as Multi-regional Clinical Trial (MRCT) for China registration.  Additionally, the CFDA has started the revision of the “Drug Administration Law” which is in place to ensure drug quality and safety.  These changes will continue to drive the evolution of the Chinese regulatory environment, directly impacting the strategy, planning and execution of the pharmaceutical companies in the development and registration of new products in China.  In this webinar, experts will review some of these regulatory changes, discuss the potential impact and share insight on how to address issues arising from these changes.

Presentations on
Recent and Upcoming Changes in Law, Regulation and Regulatory Practice
Industry’s Response and Strategies


Who Should Attend 

Professionals involved in:

  • Regulatory Affairs
  • Legal
  • Regulatory Policy
  • Research and Development
  • Strategic Planning
  • Clinical Development

Learning Objectives 

At the conclusion of this webinar, participants should be able to:

  • Describe the recent and upcoming key changes in Chinese drug regulation and regulatory review practice
  • Explain the potential impact to the industry of these changes
  • Discuss strategies to address issues arising from these changes


Contact Information 

Printable Registration Form

Registration Questions
Toll Free 1.888.257.6457
Phone +1.215.442.6100
Fax +1.215.442.6199
Monday-Friday 8:30AM-8:00PM ET

For further information, contact
Carolyn Callahan
Phone +1.215.442.6194
Fax +1.215.442.6199

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Cancellations:  No refunds will be provided in the event of a participant’s cancellation since all costs for this webinar have been prepaid by DIA. DIA reserves the right to modify or cancel programs and/or substitute presenters or panelists. DIA is not responsible for failure to deliver programs due to circumstances beyond its control.

Participants with Disabilities: Reasonable accommodations will be made available to persons with disabilities who attend an educational activity. Contact the DIA office in writing at least 15 days prior to event to indicate your needs.

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Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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