Medical Device Regulations – Materiovigilance Program of India – News Letter from IPC
News Letter from IPC on Materiovigilance Program is shared below for information.
Since Medical Devices are brought under Full Regulations in the country, one of the mandatory Regulatory Requirement is Market Surveillance by Regulator .
Read the news letter shared below for more information
Workshop on Key Role of In-Vitro Diagnostic Medical Device Stakeholders in Materiovigilance Programme of India
Indian Pharmacopoeia Commission is organising a Workshop on “Key Role of In-Vitro Diagnostic Medical Device Stakeholders in Materiovigilance Programme of India” on Friday, July 22, 2022 between 10 am to 4 pm at Indian Pharmacopoeia Commission (IPC), Ghaziabad, (U.P).
Total seats: 40, Registration will be accepted based on first come first serve basis.
Registration fee is Rs.2000 inclusive of GST. Last date for registration is July 20 2022. The objective of the workshop is to create awareness about the regulation and safety surveillance system of medical devices in India among in-vitro diagnostic medical device manufacturers, distributors, importers and researchers in order to promote the safety of in-vitro diagnostic medical devices.
Date : July 22, 2022 , Friday
Time : 10 am to 4 pm
Place : Indian Pharmacopoeia Commission, Ghaziabad
Last date for registration is July 20, 2022
Contact Number :+ 91 – 6386185827
Email Id : firstname.lastname@example.org