Authorization
Emergency Use Authorization (FDA) or Conditional Marketing Authorization (EMA)
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All vaccines follow the same testing processes, whether they are approved for emergency use or through a typical license. Clinical trials are conducted in three phases. In Phase 1, the vaccine is given to a small number of generally healthy people to assess its safety and effectiveness. vaccine.unchealthcare.org |
Foi retirado, tendo uma cópia em:
Na DGS, fizeram outro esquema, a representar de outra forma:


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