and what rights they have as research subjects. The consent form is one part of the dialogue that investigators have with each subject. It is recommended that forms for adult subjects be written at a ...

Please make sure each statement of the consent form is read and initialled by the person signing the form. They should then print, date and sign the bottom of the form and so should the professional ...

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

a model consent form included in the protocol and listed in the Table of Contents of the protocol with the same wording, or in the contract or agreement. An explanation of whom to contact for answers ...

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf ... and their probability as a direct result of participation in the research and/or ...

A waiver of the need for subjects to sign a consent form can be granted if any one of the following three conditions are met: The only record linking the subject and the research would be the consent ...