To perform a clinical investigation in India, securing permission from the CDSCO is non-negotiable. A detailed study protocol has to be developed keeping patient safety in mind. The clinical investigation plan should comply with the ethical principles and applicable...
Medical device manufacturers/importers who wish to conduct a clinical investigation in India need to obtain permission from the CLA. The CLA is the Central Licensing Authority (CLA) and functions under the CDSCO. The CDSCO is the Central Drugs Standard Control...
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