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
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.
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
Permission for Loan License to Manufacture Class A & B In- Vitro Diagnostics in India
Cliniexperts provides you with a one-stop solution for your IVD products needs right from test or loan licenses to manufacturing and post-marketing licenses.