A document with important information about a medical procedure or treatment, a clinical trial, or genetic testing. It also includes information on possible risks and benefits.
I participant name, agree to participate or agree to participation of my child participant name in the research project titled project title, conducted by researcher(s) name who has (have) discussed the research project with me. I have received, read and kept a copy of the information letter/plain language statement.
Consent Form Templates The Consent Form used in a study should be edited to match requirements of the specific study: It should include information about the investigator, the topic under study, and a clear description of purpose, risks, and benefits.
The Consent Form provides an employer's disclosure of information, rights and rules pertaining to the background check and obtains the consumer's authorization to run the background check.
The Short Form Consent Document is written in a language the non-English speaking subject or their Legally Authorized Representative can read and understand. It summarizes the information the investigator must tell the participant before consent, but it does not contain study-specific information.
The consent form should include the following statements: I understand that my participation is voluntary, that I can choose not to participate in part or all of the project, and that I can withdraw at any stage of the project without being penalized or disadvantaged in any way. I agree to take part in this study.