Regulations for Good Clinical Practice Article 82
The auditing procedures should comply with:1.The auditing procedures is conducted in accordance with the sponsor's written procedures on what to audit, how to audit, the frequency of audits, and the form and content of audit reports.2.The sponsor's audit plan and procedures for a trial audit should be guided by the importance of the trial, the number of subjects in the trial, the type and complexity of the trial, the level of risks to the trial subjects, and any identified problem(s).3.The observations and findings of the auditor(s) should be documented in writing.4.To preserve the independence and value of the audit function, the Competent Authority should not routinely request the audit reports, except when evidence of serious non-compliance with this Regulations exists, or in the course of legal proceedings, the Competent Authority may seek access to an audit report on a case by case basis.5.The sponsor should provide an audit certificate.
中文原文 藥品優良臨床試驗作業準則第82條
稽核程序應符合下列規定:
一、應稽核之部分、如何稽核、稽核次數及稽核報告之內容及形式,應依照試驗委託者之標準作業程序執行。
二、試驗委託者稽核之計畫及程序,應依據試驗之重要性、受試者人數、試驗之種類及複雜性、受試者風險,及其他提出之問題訂定。
三、稽核者之觀察和發現,應以書面記錄。
四、為維護稽核功能之獨立性及其價值,主管機關不得要求提供定期稽核報告。
但證明有嚴重違反本準則之規定或因應司法程序,主管機關得要求個別稽核報告五、試驗委託者應提供稽核憑證。
一、應稽核之部分、如何稽核、稽核次數及稽核報告之內容及形式,應依照試驗委託者之標準作業程序執行。
二、試驗委託者稽核之計畫及程序,應依據試驗之重要性、受試者人數、試驗之種類及複雜性、受試者風險,及其他提出之問題訂定。
三、稽核者之觀察和發現,應以書面記錄。
四、為維護稽核功能之獨立性及其價值,主管機關不得要求提供定期稽核報告。
但證明有嚴重違反本準則之規定或因應司法程序,主管機關得要求個別稽核報告五、試驗委託者應提供稽核憑證。