Regulations for Good Clinical Practice Article 18
None of the informed consent form and any other written information to be provided to subjects shall contain any language that causes the subject or the subject's legally acceptable representative to waive or to appear to waive any legal rights, or that releases or appears to release the investigator, the institution, the sponsor, or their agents from liability for negligence.Statements in contradiction to the rules specified in the preceding paragraph are invalid.
中文原文 藥品優良臨床試驗作業準則第18條
受試者同意書及提供受試者之任何其他書面資料，不得有任何會造成受試者、法定代理人或有同意權之人放棄其法定權利，或免除試驗主持人、試驗機構、試驗委託者或其代理商責任之記載。
違背前項規定之記載，無效。
違背前項規定之記載，無效。