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TEMPLATE INFORMED CONSENT FORM FOR RESEARCH WITH HUMAN SUBJECTSProtocol Title: Genetic Epidemiology of Chronic Obstructive Pulmonary Disease: The Cologne Study Principal Investigator: ___Introduction
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How to fill out template informed consent form

01
Start by providing the title of the study at the top of the form.
02
Include a brief description of the research being conducted and the purpose of the study.
03
Clearly outline the procedures involved in the study and what participants can expect.
04
Include information about the risks and benefits of participating in the study.
05
Provide details about confidentiality and how participant data will be protected.
06
Include a section for participants to provide their consent by signing and dating the form.
07
Make sure to include contact information for the researcher in case participants have any questions.
08
Have a witness present to also sign and date the form to verify that the participant provided informed consent.

Who needs template informed consent form?

01
Researchers conducting studies that involve human participants need to use a template informed consent form to ensure that participants have all the necessary information about the study before agreeing to participate.
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The template informed consent form is a standardized document that explains the research study, risks involved, and procedures to the participants.
Researchers conducting a study involving human subjects are required to file the template informed consent form with the appropriate review board.
The template informed consent form should be filled out with relevant information about the study, risks, procedures, and participant rights.
The purpose of the template informed consent form is to ensure that participants are fully informed about the study and voluntarily agree to participate.
The template informed consent form must include information about the study, risks involved, procedures, participant rights, and contact information for questions.
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