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          乐旺娱乐城

           
          400-876-8783
          服務熱線:?
          印度器械注冊
          Medical Device Registration Certificate in Form 41 (For Foreign Manufacturer)
          · Determine your device fits or not into the list of notified Medical Devices regulated under Drugs and Cosmetics Act, 1940; and Rules, 1945.
          · Coordinate the device registration and approval process with Indian Medical Device Regulators (DCG(I)/CDSCO)
          · Preparation of all necessary documents for the product registration application including Forms 40.
          · Suggesting appointing an Indian Agent as your official representative.
          · Submission of Site Master File and Device Master File as needed.
          · Coordinate with the DCG(I)/CDSCO to address follow up questions and monitor progress

          郵箱:info@sungoglobal.com


          服務熱線: 400-876-8783  

               021-68828052


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          乐旺娱乐城