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Medical device clinical trials consulting service

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Description

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

SFDA, MEDICAL DEVICE,

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Osmunda Medical Device Consulting CO.LTD

medical device registration co

Address: 7th Floor,JinGui business center,CongYun road No.982,Baiyun,
Guangzhou, Guangdong
China,

Tel: 0086-020-62321333
Fax:

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