Ablation Devices Now Require Registration in India
The India Ministry of Health and Family Welfare added ablation devices to the list of notified medical device that require registration.
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The India Ministry of Health and Family Welfare added ablation devices to the list of notified medical device that require registration.
More companies are setting up a subsidiary or using an independent license holder in order navigate the highly rationalized Indian market.
The Drugs Controller General of India (DCGI) announced on May 1, 2016 that the SUGAM online application submission system, in use since November 2015 for pharmaceutical registration, would be extended to medical device and IVD device submissions (e.g., registration and import license applications).
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