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The role of academia and professional organisations in research, from marketing authorisation to patient use and beyond in varying settings

  • At: 2018 FIP Congress in Glasgow (Scotland)
  • Type: Presentation
  • By: CHEN, Timothy (The University of Sydney, Australia)
  • Abstract:

    National regulators have the responsibility of assessing medicines for safety and efficacy prior to the approval. Following this process, some health care professionals and consumers may have an assumption that medicine effectiveness is guaranteed and that safety or absence of adverse effects is assured. The objective of this presentation is to


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Last update 4 October 2019

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