Medical device clinical trials consulting service - FFF522544
Medical device clinical trials consulting service For Sale, Most Competitive Price, Fast Delivery, Custom Service, Wholesale Medical device clinical trials consulting service , Made in China, High Quality Products!, China SFDA, MEDICAL DEVICE Supplier, Manufacturer.
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
Osmunda Medical Device Consulting CO.LTD
Address: 7th Floor,JinGui business center,CongYun road No.982,Baiyun, Guangzhou, Guangdong, China,
Tel: 0086-020-62321333
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.
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SFDA Registration
FFF5225
