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Understanding and Implementing Best Ethics Practices in Clinical Research

 
  November 03, 2011  
     
 
Peking University Health Science Center , Beijing, China
Dec 13 2011 8:00AM - Dec 14 2011 5:00PM


With the continually increase of clinical studies in China, ethical considerations and good practices in clinical research and studies have received more attention by regulators, investigators/practitioners, and study sponsors. Good ethics practice plays an important role in both protecting and benefiting patients through medical and pharmaceutical science and technology development.

This two-day training course is an interactive forum that provides in-depth knowledge, international and China regulatory guidelines, and practical solutions to assist participants to gain a better understanding of the ethical requirement and to implement best ethics practices in clinical research.  The course is designed by subject matter experts with examples from real-life experience. The instructors will compare Chinese requirements and ICH/European/US requirements with special focus on ethical review, the informed consent process, and risk management.

Event Code:
11980
 
 
Organized by: DIA China
Invited Speakers: See website for speaker information
 
Deadline for Abstracts: Call contact
 
Registration:
Gateway Plaza A, Room 1155, 18 XiaGuangLi, North Road Third
Ring| Chaoyang District, Beijing, 100027, China
Tel: +86-10-59231222 Fax: +86-10-59231180
E-mail: fei.XIE@diachina.org
 
   
 
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