ABOUT US

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.

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

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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.

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