Regulations for Good Clinical Practice Article 92
The investigator or the institution should be responsible for the accountability and storage of the investigational product(s).The investigator or the institution may assign some or all of the duties for investigational product(s) accountability and storage at the trial site(s) to designated pharmacists or other appropriate individuals.
中文原文 藥品優良臨床試驗作業準則第92條
試驗主持人或試驗機構應負責試驗藥品之點收及保存。
試驗主持人或試驗機構得指派專責藥師或適當人員負責部分或全部試驗藥品之點收及保存。
試驗主持人或試驗機構得指派專責藥師或適當人員負責部分或全部試驗藥品之點收及保存。