Common use of Informed Consent Form Clause in Contracts

Informed Consent Form. Site agrees to use an informed consent form that has been approved by Sponsor and is in accordance with applicable regulations and the requirements of the Ethics Committee for Multicentrics Trials (“ECMT”) and Local Ethics Committees (“LEC”), jointly Ethics Committees (“EC”) that is responsible for reviewing the Study. Site shall obtain the prior written informed consent of each Study Subject.

Appears in 1 contract

Sources: Clinical Trial Agreement

Informed Consent Form. Site agrees to warrants that Site will only use an informed consent form that has been approved by Sponsor and is in accordance with applicable regulations and the requirements of the Ethics Committee for Multicentrics Trials (“ECMT”) and Local Ethics Committees (“LEC”), jointly Ethics Committees (“EC”) that is responsible for reviewing the Study. Site Investigator shall obtain the prior written informed consent of each Study SubjectSubject or his/her legally authorized representative, in accordance with applicable laws and regulations.

Appears in 1 contract

Sources: Clinical Trial Agreement

Informed Consent Form. Site agrees to use an informed consent form that has been approved by Sponsor and is in accordance with applicable regulations and the requirements of the Ethics Committee for Multicentrics Trials (“ECMT”) and Local Ethics Committees (“LEC), jointly Ethics Committees (“EC”) that is responsible for reviewing the Study. Site Investigator shall obtain the prior written informed consent of each Study Subject.

Appears in 1 contract

Sources: Clinical Trial Agreement