Health ministry to set up a panel to review medical device-related adverse events
Medical devices comprise electronic equipment, implants, consumables and disposables, surgical instruments and in-vitro ...
来自MSN2 个月
India mandates faster reporting of drug side effects
DGCI rules already require manufacturers, importers, and marketers of pharmaceutical products in India to report adverse events involving ... Control Organization (CDSCO). Per Pubmed, a medical ...