MEDATEQ LABS provide medical device regulatory services to our client’s assistance with application and licensing procedures related to Medical Devices. Regulatory bodies classify medical devices based upon the associated risk and have defined relatively easy procedures for license applications. The medical devices categorized by respective government central and state regulatory authorities into A, B, C and D classes. And also for import of medical devices.
MEDATEQ LABS helps to Overseas clients that provide a responsible authorized agent for the import and register their products in India including compliance to the provisions of the Drugs and Cosmetics Acts in all respects.