Indian Pharmacopoeia Commission as National Coordination Centre (NCC) for Materiovigilance Programme of India (MvPI) has developed the following tools for better medical devices adverse event reporting and management in consultation of CDSCO and NHSRC.
- Medical Device Adverse Event Reporting form version 1.1 (Please click) (Annexure I)
- Field Safety Corrective Action Form (Please click). (Annexure II)
- Registered Medical Devices Information Sharing Portal (Please click). (Annexure III)
Now these tools are available for comment/suggestions for stakeholders. Stakeholders are requested to offer their comments if any on or before 31st December 2018