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MATERIOVIGILANCE PROGRAMME OF INDIA
Medical gear firms told to 'promptly' flag adverse casesIndian medical device firms must now promptly report all adverse events, both serious and non-serious, to the government's Materiovigilance...- Set up system for reporting adverse events: Regulator to medical device companiesThe government mandates companies to carry out post-market surveillance (PMS) of medical devices with an aim to ensure the safety and perfo...
- Health ministry to organise 'Chintan Shivir' to explore ways to build trust on Indian drugs"The aim is to build trust and confidence on the quality of Indian drugs, cosmetics and medical devices in the domestic and global markets."
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