Regulations for Good Clinical Practice Article 32
The investigator shall be aware of, and shall comply with, this Regulations and the applicable regulatory requirements.
中文原文 藥品優良臨床試驗作業準則第32條
試驗主持人應明瞭並遵守本準則及相關法規之要求。
English translation for reference only; the Chinese text prevails. Not legal advice.