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Approved: 29Nov2016INFORMATION SHEET AND CONSENT FORM AND HIPAA AUTHORIZATION Study Title:A RANDOMIZED, DoubleClick, PARALLEL GROUP, MULTIMETER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF BEMPEDOIC ACID

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What is information sheet and consent?

Information sheet and consent is a document that outlines the details of a research study, including the purpose, risks, benefits, and procedures involved. It also includes a section for participants to provide their consent to participate in the study.

Who is required to file information sheet and consent?

Researchers conducting a study that involves human participants are required to file an information sheet and consent.

How to fill out information sheet and consent?

To fill out an information sheet and consent, researchers must include all relevant details about the study in a clear and concise manner. Participants must also be given adequate time to review the document and ask any questions before providing their consent.

What is the purpose of information sheet and consent?

The purpose of an information sheet and consent is to ensure that participants are fully informed about the study they are participating in, including any risks or benefits involved. It also serves as documentation of the participant's voluntary agreement to participate.

What information must be reported on information sheet and consent?

The information sheet and consent must include details such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality measures, contact information for the researcher, and the participant's rights.

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