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complete procedure to meet

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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Health Ministry Draft Notification To Add 16 Drugs as OTC Under Schedule K of Drugs Rules, 1945

According to the latest draft gazette notification, G. S. R. 393 (E), released on 25-05-2022, The Ministry of Health and Family Welfare (MoHFW) has circulated a notification by revising Schedule K of...

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New Rules added by the CLA on suspension and cancellation of license of imported Medical Devices.

The Ministry of Health and Family Welfare (Department of Health and Family Welfare) under the Government of India, on 18th January 2022, G.S.R.78 (E) released an official gazette with a few new...

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Manufacturing And Product Development Support For Class A Medical Devices/IVD’s

Class A Medical Devices / IVDs – Class A medical devices / IVDs are medical equipment that has low risk to the patients and public health risks. Class A medical devices /...

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