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FDA URGES VIRTUAL PATIENT VISITS

Focus: GS-III Science and Technology, To be used as example in Science and Technology Mains Paper

Why in news?

  • The U.S. Food and Drug Administration on March 18 2020, recommended switching to virtual patient visits instead of in-person monitoring for clinical studies, as signs emerge that the rapid spread of the coronavirus outbreak is disrupting trials.
  • The companies said these measures were taken to ensure the safety of the patients being tested and the medical staff.
  • The FDA said the outbreak may impact clinical trials of products including drugs and devices, as travel limitations and other considerations cause protocol deviations.
  • The restrictions have begun to disrupt the global pharmaceutical industry, as companies cancel public meetings.

Virtual Visits

  • Virtual healthcare refers to the “virtual visits” that take place between patients and clinicians via communications technology — the video and audio connectivity that allows “virtual” meetings to occur in real time, from virtually any location.
  • A virtual visit can be a videoconference between a doctor and a patient at home.
  • It could mean that a patient can interact with an offsite medical specialist via a high-definition conference hook-up at his or her local clinic, instead of traveling to another city.
  • It can also give patients the chance to more readily find qualified second opinions online.



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December 2022
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