Vigilance & Adverse Event Reporting
5 items
Post-Market Surveillance
4 items
Recalls & Field Safety Actions
4 items
Labelling & Advertising
4 items
Unique Device Identification (UDI)
5 items
Post-Market — Staying compliant
Post-market obligations in India under the Medical Devices Rules 2017: vigilance and adverse event reporting (MDVP), post-market surveillance, recalls and field safety actions, labelling and advertising, and UDI.