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Approved Informed Consent FormsProject Title: Enhancing Male Participation in Interventions to Prevent Unintended Pregnancy (CHARM2) NCT number: NCT03514914 Date of document creation: 4/4/2019 Date
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How to fill out approved informed consent forms

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Read the informed consent form thoroughly to understand the purpose and procedures involved.
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Provide accurate and truthful information in the required fields.
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Sign and date the form in the designated sections.
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Ask any questions or seek clarification from the research team if needed.
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Keep a copy of the signed informed consent form for your records.

Who needs approved informed consent forms?

01
Individuals participating in research studies or clinical trials.
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Patients undergoing medical treatments or procedures.
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Participants in experimental programs or interventions.
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Approved informed consent forms are documents that outline the risks, benefits, and procedures of a research study, and are signed by the participant to acknowledge their understanding and agreement to participate.
Researchers conducting a study requiring informed consent are required to file approved informed consent forms.
Approved informed consent forms are typically filled out by the researcher or study coordinator with input from the participant. The form should be clear, concise, and include all necessary information.
The purpose of approved informed consent forms is to ensure that participants are fully informed about the study they are participating in, including any potential risks or benefits, and to document their voluntary agreement to participate.
Approved informed consent forms must include information about the study objectives, procedures, risks, benefits, confidentiality measures, contact information for questions, and the opportunity for the participant to withdraw from the study at any time.
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