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Serious adverse event monitoring and reporting system in the institutional review board of changhua christian hospital

  • At: 2008 FIP Congress in Basel (Switzerland)
  • Type: Poster
  • By: CHEN, Yi-Ju (Changhua Christian Hospital, Changhua, China Taiwan)
  • Co-author(s): Tsai, Pei-Ling (Changhua Christian Hospital, CHANGHUA, China Taiwan)
    Liao, Shu-Chen (Changhua Christian Hospital, CHANGHUA, China Taiwan)
    Hsiao, Hui-Fang (Changhua Christian Hospital, CHANGHUA, China Taiwan)
    Huang, Luke Yee-Wen (Changhua Christian Hospital, CHANGHUA, China Taiwan)
    Chien, Su-Yu (Changhua Christian Hospital, CHANGHUA, China Taiwan)
  • Abstract:

    Introduction:

    In order to protect the participating subjects in clinical trials, institutional review board (IRB) monitors the safety of study continually. When a serious adverse event (SAE) occurred, the principle investigator is obligated to inform IRB. Pharmacists in IRB assess the reported information to evaluate its severity. The IRB..

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Last update 4 October 2019

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