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Medical Device Clinical Trials Consulting Service In China - China

price: contact company for price

Osmunda can offer the following clinical trials service:

1.Clinical trials content

2.Select and confirm the clinical trials site

3.Design for clinical trails plan and case report form

4.Organize the cinical kick-off meeting, middle phase meeting and sum-up meeting

5.Tracing and supervising the clinical trials process

Clinical trials process:

1.Conform the clinical commission requirements from the applicants

2.Draft the agreement, including the number of the trial cases, time duration, purpose and consulting fee, and sign the commission agreement by the confirmation of both side.

3.Select and confirm the clinical trial sites

4.Sign the clinical trials plan and clinical trails agreement

5.Design and perfect the clinical trial plan

6.Submit the clinical trials plan to the ethics committee for approval

7.Submit the clinical trials documents

8.Clinical report composed by the clinical site and the origin material required to be archived.

9.Clinical trials report

Medical Device Clinical Trials Consulting Service In China

Please see our contact information below


Company Contact:


  • Phone: 862062321333

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

  • Email: Email


Published date: September 7, 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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