Common use of Investigator Obligations Clause in Contracts

Investigator Obligations. As indicated on FDA Form 1572, the Principal Investigator is responsible for ensuring that all study site personnel, including Sub-Investigators and other study staff members, adhere to all FDA regulations and guidelines regarding clinical trials both during and after study completion.

Investigator Obligations. As indicated on FDA Form 1572, the Principal Investigator is responsible for ensuring the conduct of the clinical trial at the site and is responsible for personally overseeing the treatment of all study patients. The Principal Investigator must assure that all study site personnel, including Sub-Investigators investigators and other study staff members, adhere to the study protocol and to all FDA regulations and guidelines regarding clinical trials both during and after study completion.