Regulations for Good Clinical Practice Article 37
The investigator should have available an adequate number of qualified staff and adequate facilities to conduct the trial properly and safely.The investigator shall supervise the individual and party delegated by him/her to perform duties related to the trial.
中文原文 藥品優良臨床試驗作業準則第37條
試驗主持人應有充分之合格試驗相關人員及設施，以適當並安全的執行試驗。
試驗主持人應監督其授權執行與試驗相關業務之人員及單位。
試驗主持人應監督其授權執行與試驗相關業務之人員及單位。