The items which are not restricted can be easily imported but, the ones which are restricted need to get approval from DGFT (Directorate General of Foreign Trade). We at CliniExperts provide consultation and assistance to our clients regarding the import of restricted items in India. We provide the following services:
Not only at DGFT, have we helped our clients in liaisoning process at Central Insecticides Board and registration committee, Faridabad.
Traditional Medical Device regulation assumes a fixed product: what’s approved is what ships, indefinitely, until a formal change is filed and reviewed. Adaptive AI and machine learning algorithms b..
Getting a Cosmetic product registered and onto shelves in India is only half the job. Once a product is in the market, the Cosmetics Rules, 2020 place ongoing duties on manufacturers and Importers to ..
Although software intended for Medical purposes has been regulated in India since the implementation of MDR, 2017 Rules. CDSCO’s Guidance Document on Medical Device Software (Doc No. CDSCO/MD/GD..
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