International Medical Device Regulators Forum

International Medical Device Regulators Forum is a group of global medical device regulators whose aim is to speed up the adoption of international medical device regulatory harmonisation and convergence.

International Medical Device Regulators Forum

About International Medical Device Regulators Forum:

  • The IMDRF was established in 2011.
  • It is a group of global medical device regulators whose aim is to speed up the adoption of international medical device regulatory harmonisation and convergence.
  • Members: Its members include national regulatory authorities of the U.S., Australia, Canada, the European Union, Japan, the United Kingdom, Brazil, Russia, China, South Korea, Singapore and the World Health Organization (WHO).
  • The membership helps to harmonize regulatory requirements across the globe, which reduces the complexity for manufacturers and helps in safeguarding public health by promoting collaboration, harmonizing regulations, and promoting convergence.
  • It also helps to support innovation and timely access to new medical devices.
  • Significance to India
    • India will participate in IMDRF Open Sessions to have information exchange on technical topics with other regulators, discussion on latest medical device regulatory strategies and trends, provide feedback on India’s experience and perspectives.
    • This will strengthen the CDSCO’s medical device regulatory system, helping meet emerging technical challenges that are increasingly diverse, to ensure protection of public health and safety, and continue to maintain the goal of international recognition for its Medical Device regulation.

Q1:What is the World Health Organisation?

The World Health Organization (WHO), established in 1948, is a specialized agency of the United Nations that connects nations, partners and people to promote health, keep the world safe and serve the vulnerable – so everyone, everywhere can attain the highest level of health. 

Source: India becomes affiliate member of International Medical Device Regulators Forum

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