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印度器械注册
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

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日本法规
巴西ANVISA
韩国KFDA
俄罗斯医疗器械注册
印度器械注册
加拿大法规

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