The FDA is set to exempt certain types of software from regulatory oversight as it reconsiders its approach to products on the fringes of the medical device sector. Officials at the agency set out ...

The domestic medical devices industry in the country has suggested that the definition of manufacturer in the draft New Drugs, Medical Devices and Cosmetics (NDMDC) Bill, 2022, to be changed with more ...

In order to support indigenous medical device industry, the Association of Indian Medical Device Industry (AiMeD) has urged the Centre to change the definition of manufacturers in the Guidance ...