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Interpretation On Clinical Trial Regulation Of Medical Device Seminar Will Open In December - China

price: contact company for price

Supervision of clinical trial of medical device in China is stricter and

stricter. With the latest medical device regulation coming into

practice, more concrete clinical trial methods of medical device and its

related regulations will be promulgated.

Interpretation and practice of Clinical Trial Regulation of Medical Device Seminar held by the Guangdong Medical Device Quality Surveillance and Test Institute, China Quality Association for Pharmaceuticals (CQAP) and Osmunda Medical Device Consulting Organization will open on December 18th to embed the regulation requirement of clinical trial into medical device enterprises in domestic and abroad and to explore the prospect of clinical trial regulation of medical device.

Three themes are as follows:

1. Theme: Interpretation on clinical trial regulation of medical device and analysis of its latest development

Speaker: experts from Department of Medical Device supervise of Guangdong Food and Drug Administration

2. Problems of clinical trial of medical device performed in the hospital and its solutions

Speaker: professors from The Second Affiliated Hospital of Guangzhou Medical College

3. Designs and case studies of clinical trial of medical device

Speaker: Directors of Clinical Trial Center from Osmunda Medical Device Consulting Organization

For more on this , see 020-62321333,www.osmundacn.com

Interpretation On Clinical Trial Regulation Of Medical Device Seminar Will Open In December

For any questions and needs please contact us below


Company Contact:


  • Phone: 862062321333

  • Address: 7th Floor, Jingui Business Building, No.982 Congyu, Guangzhou, China

  • Email: Email


Published date: November 26, 2012 -

  • Business Description: Osmunda Medical Device Consulting Organization

    (Guangzhou, Beijing, Shanghai, Suzhou, Shenzhen and Jinan) is the

    largest and most professional consulting company in the field of medical

    device in China. All Osmunda Consultant team members are from sizeable

    medical devices enterprises, well known notified bodies and testing

    organizations. We are well versed in global various medical device

    quality system certification and product registration, such as SFDA

    registration, QSR 820 system, FDA registration, ISO 13485 system, CE

    certification etc. Our service includes clean room design, clinical

    trail, third party audit, training of regulations and standards, etc.

    Our headquarters is in Guangzhou, and we have five branch offices (Beijing, Shanghai, Suzhou, Shenzhen, Jinan) which could provide high speed local services and communication. By far, Osmunda has successfully assisted nearly 1,200 domestic and foreign enterprises in achieving various medical devices registration and certification. We will be your trustful partner and your most professional guide.

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