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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