Medical Device Class C D Manufacturing License/ Registration - Class C D Medical Device Regulatory Services. Medical Device Class C D Regulatory Compliance and Licensing Services by CliniExperts. Call +91 7672005050

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India Regulatory Expert Video Series. Explore amazing helpful videos for regulatory services for medical device, cosmetics, biologicals and legal metrology

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Permission to conduct Clinical Performance Evaluation of In-vitro diagnostic kit / New In Vitro Diagnostic Medical Device Performance Evaluation for Importer/Manufacturer. Call +91 7672005050

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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

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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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Permission for Loan License to Manufacture Class C & D In- Vitro Diagnostics in India – MD-8 & MD-10
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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Registration of Manufacturers, Importers and Packers (Packaging and Warehouse Registration) under Rule 27 in India
CliniExperts provides regulatory solutions and has a current Drug Wholesale License for bringing medical devices into India.

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POST APPROVAL CHANGES For Cosmetics
Get authorized agent support for all your post approval changes to Cosmetic substance for already approved Cosmetic manufacturing site

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