MVPI

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Across
  1. 4. – Indian certification scheme for ensuring quality of medical devices.
  2. 6. – Online system used in India to report adverse events from medical devices.
  3. 8. – Any undesirable experience associated with the use of a medical device.
  4. 9. – Surveillance phase after a device is approved and released to market.
  5. 10. – Any instrument or apparatus used for diagnosis, prevention, or treatment.
  6. 11. – Regulatory authority in India overseeing drugs and medical devices.
Down
  1. 1. – Science and activities related to detecting adverse effects of medical devices.
  2. 2. – Regulatory action to remove unsafe or defective medical potential harms related to device use.
  3. 3. – Organization designated to assess the conformity of devices before marketing.
  4. 5. – Systematic monitoring of drug safety, often paralleled with materiovigilance.
  5. 7. – Indian program launched to monitor medical device-associated adverse events.