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Standard Operating Procedure (SOP) for Recruiting and Consenting Patients into Clinical Researcher Completion by SOP AuthorReference Number/RD SOP/005VersionV1.1 07 Apr 2016Document Author(s)Emma

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What is recruiting and consenting patients?

Recruiting and consenting patients is the process of identifying potential participants for a clinical trial, explaining the study to them, obtaining their informed consent, and enrolling them in the trial.

Who is required to file recruiting and consenting patients?

The principal investigator or sponsor of the clinical trial is required to file recruiting and consenting patients.

How to fill out recruiting and consenting patients?

Recruiting and consenting patients forms are typically filled out by the research team, including the principal investigator, study coordinators, and other staff members involved in patient recruitment and enrollment.

What is the purpose of recruiting and consenting patients?

The purpose of recruiting and consenting patients is to ensure that participants understand the study, its risks and benefits, and voluntarily agree to participate.

What information must be reported on recruiting and consenting patients?

Recruiting and consenting patients forms typically include details about the study, potential risks and benefits, the consent process, and participant contact information.

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