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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.. The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.
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Last update 4 October 2019