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STUDY00012248 Approval: 9/2/2020 Approval End Date: 9/1/2021Version Date: 10/28/2019CONSENT FOR RESEARCH Penn State College of Medicine Penn State Health Title of Project:Effect of formal contraception

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Review the master informed consent form and familiarize yourself with its contents.

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Fill out all the sections of the form accurately and completely.

03

Make sure to include all necessary information such as participant's name, date, study details, risks and benefits, confidentiality agreements, etc.

04

Provide explanations or answer any questions the participant may have before they sign the form.

05

Have the participant sign and date the form to indicate their informed consent to participate in the study.

Who needs master informed consent form?

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Researchers conducting studies involving human participants.

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What is master informed consent form?

The master informed consent form is a document that outlines the details of a study and the potential risks and benefits involved. It is used to ensure that participants are aware of the study procedures and give their voluntary consent to participate.

Who is required to file master informed consent form?

Researchers and study coordinators are required to file the master informed consent form to obtain approval from an ethics committee or institutional review board before starting a study involving human subjects.

How to fill out master informed consent form?

The master informed consent form should be filled out by providing accurate and comprehensive information about the study, including the objectives, procedures, risks, benefits, confidentiality measures, and participant rights. Participants should be given ample time to read the form and ask any questions before signing it.

What is the purpose of master informed consent form?

The purpose of the master informed consent form is to protect the rights and welfare of participants in a research study by ensuring that they are fully informed about the study procedures and potential risks, and that they voluntarily agree to participate.

What information must be reported on master informed consent form?

The master informed consent form must include information about the study objectives, procedures, risks, benefits, confidentiality measures, participant rights, contact information for the research team, and any compensation or incentives offered to participants.

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