Medical Device
October 25, 2023
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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March 22, 2022
An import license for new medical devices (Form MD 26 & MD 27) is a prerequisite for starting a business to sell or distribute medical devices. Having an import license gives a...
Regulatory Update
February 28, 2022
Blog
February 25, 2022
The Drugs and Cosmetics Act of 1940, as well as the rules promulgated under it, govern the safety, quality, and performance of medical devices. The Central Government has notified Medical Devices Rules,...
Blog
February 8, 2022
The Drugs and Cosmetics Act of 1940, as well as the rules promulgated under it, govern the safety, quality, and performance of medical devices. The Central Government has notified Medical Devices Rules,...
Blog
January 31, 2022
The medical devices market is growing at a fast pace along with the drug market despite all the challenges created by insufficient quality standards and other inconveniences. In India, medical devices are...
Blog
January 17, 2022
Drugs and Cosmetics Act, 1940, and Rules regulates all new medical device’s safety, quality, and performance. The Central Government has notified the new Medical Devices Rules, 2017 vide G.S.R. 78E dated January...
Regulatory Update
December 10, 2021
Blog
December 8, 2021
The Drugs and Cosmetics Act, 1940, and Rules regulate all medical devices' safety, quality, and performance. MoHFW (Ministry of Health and Family Welfare's) has issued notification vide G.S.R. 102 (E) dated 11.02.2021,...