| 摘要 |
<p><P>PROBLEM TO BE SOLVED: To provide an informed consent information management system, etc., capable of effectively reducing the burden of acquiring informed consent information required to be acquired for each research theme and each clinical trial theme. <P>SOLUTION: In this system, etc., an informed consent information managing device 100 stores sample data information of a research object person, stores informed consent information of the research object person, extracts sample data information that coincides with a research condition requested by a research institution system 400 and checks whether or not the research condition is included within the effectiveness range of informed consent information corresponding to the extracted sample data information. <P>COPYRIGHT: (C)2005,JPO&NCIPI</p> |
