Common use of Informed Consent Form Clause in Contracts

Informed Consent Form. Institution 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.

Informed Consent Form. Institution 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.

Informed Consent Form. Institution agrees to use an informed consent form that has been approved in writing by Sponsor and is in accordance with applicable regulations and the requirements of has been approved by 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. Site agrees that any revised versions of the informed consent form previously approved by the Sponsor and the EC must be approved by the Sponsor and the EC.

Informed Consent Form. Institution agrees to that the Investigator shall 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.

Informed Consent Form. Institution agrees Institutionagrees 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.

Informed Consent Form. Institution 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.

Informed Consent Form. Institution 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.

Informed Consent Form. Institution 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“LEC), jointly Ethics Committees (“„EC”) that is responsible for reviewing the Study. Site shall obtain the prior written informed consent of each Study Subject.