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Medical Device Registration in India in Form 41

Company : DKNSB Medical Device Consultant

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.

Product URL : http://dknsb.in/services/licensing-from-CDSCO.html

Last Updated : 10/31/2013

Please provide the following information and a representative of DKNSB Medical Device Consultant will contact you to assist with any questions you might have.


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