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COVID-19 Vaccines: Regulation, Allocation, & Hesitancy

Update

With several COVID-19 vaccines now making their way toward marketing approval, a number of difficult questions loom. Who should have access to the first available doses? How will companies and regulators assess safety and efficacy, including over the long term? And what does research say about the best ways for public health experts—and journalists—to communicate about the benefits and risks of COVID-19 vaccination? SciLine's on-the-record briefing addressed these issues and provided journalists with an opportunity to ask questions.

This article was published on
December 3, 2020

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Media briefing

  • Dr. Michele Andrasik, Fred Hutchinson Cancer Research Center
  • Prof. R. Alta Charo, University of Wisconsin at Madison
  • Dr. Margaret “Peggy” Hamburg, former Commissioner, U.S. Food and Drug Administration
  • SciLine Director Rick Weiss will moderate the briefing.
  • Media Release

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