The Department of Pharmaceuticals (DoP) on March 16, 2022, published the draft UCMDMP which is intended to be a voluntary code to regulate fair marketing practices by the Medical Device industry. The marketing practices of the Medical Device Sector are currently being voluntarily regulated by Uniform Code for Pharmaceuticals Marketing Practices (UCPMP) which is a […]
The Quality Council of India recently launched a local medical device certification scheme called ICMED plus, re-specifying the requirements for a quality management system for Medical devices in India which were already existing in MDR 2017 and ISO 13485. Medical Technology Association of India (MTaI), which represents leading research-based medical technology companies with large footprints […]
