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CliniExperts is an expert regulatory solutions provider based in India. It has a team of thoroughly updated and seasoned professionals that enable 360 degree regulatory support for both domestic and foreign markets.

Permission to conduct clinical investigation in India – MD22 & MD-23

CliniExperts works as an expert solution provider for regulatory processes in India. It provides 360-degree regulatory support for both domestic and foreign markets

Registration For Non-Notified In Vitro Diagnostic in India

CliniExperts holds a valid Drug Wholesale License and provides 360-degree regulatory solutions to importers and manufacturers of IVDs and other medical devices to launch their products in the Indian market.

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CliniExperts provide end-to-end support throughout the application process and submission of Form MD-8 for manufacturing the Class C and D IVDs.

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CliniExperts provides regulatory solutions and has a current Drug Wholesale License for bringing medical devices into India.

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Get authorized agent support for all your post approval changes to Cosmetic substance for already approved Cosmetic manufacturing site

Manufacture Class A & B In Vitro Diagnostics

The seasoned and updated professionals at CliniExperts will assist you in every step of the application process in filing the FORM MD-3 and obtaining the Grant of License to manufacture Class A & B IVDs in FORM MD-5