Complete Procedure to Meet the CDSCO License Mandate of Class C & D Non-Notified Medical Devices
Overview of the CDSCO License Mandate The Central Drugs Standard Control Organisation (CDSCO) is the regulatory body that manages medical device registration in India under the Ministry of Health & Family Welfare. The main aim of CDSCO is to ensure that medical devices are...
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As per the order dated 10th October 2022, FSSAI notified that registration of Foreign Food Manufacturing Facilities (ReFoM) intending to export Egg powder; Nutraceuticals; Meat & meat items, including fish, poultry & their...
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Active pharmaceutical ingredient (API) is defined as the component of a drug that is active biologically and is present in the tablet, injection, capsule, or cream and produces the intended health effect....
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Drug Technical Advisory Board (DTAB): The Drug Technical Advisory Board is a committee constituted as per the provisions of the Drugs and Cosmetics Act, 1940. Drug Technical Advisory Board is a part...
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FSSAI is an autonomous statutory body established by the Ministry of Health & Family Welfare, Government of India. FSSAI works under the regulations of the Food Safety and Standards Act 2006. It...
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