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DRS handholds and facilitate you in the Indian regulatory pathway of Medical Device & IVDs.


The Management of DRS provides services pertaining to the development, documentation, testing, approval, manufacturing, and importing of the medical devices and IVDs sector at a cost-effective method and speedy approvals.

DRS Management intends to pursue modern quality management through an adequate organizational structure and an optimal organization of resources; 

DRS articulates its strategy by Compliance with mandatory national regulations and technical regulations on the basis of the data relating to the Customer's needs and, where possible.

DRS provides the complete regulatory provisions in the simplest method and a phase-wise pathway for regulation of medical devices is established.


"Our vision is to acquire speedy approvals to enable clients to achieve their objective of a timely and successful product launch."

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