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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For any Foreign Medical Device company seeking to sell its devices in India, obtaining an Import License from CDSCO is a mandatory Regulatory requirement. The two central application forms in this process...
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India's Emerging Advanced Therapy Landscape Cell and Gene therapies — and chimeric antigen receptor T-cell (CAR-T) therapies in particular — represent one of the most transformative frontiers in modern medicine. With a...
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For global Pharmaceutical companies evaluating emerging market expansion, three regions consistently dominate strategic discussions: India, ASEAN, and the GCC. Each offers compelling growth characteristics. Each carries a distinct regulatory architecture, commercial structure,...
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The Categorisation Problem Of all the challenges in India's Cosmetic Import registration process, product categorisation is one of the most underestimated. Under the Cosmetics Rules, 2020, CDSCO has prescribed 80 Cosmetic categories...
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