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Ten Tips for Writing Compliant
Participant Materials



Sponsors, CROs, and investigators developing participant materials should download this whitepaper to ensure those materials are the most effective, useful, and compliant they can be. Our participant materials experts offer insights on:
  • Abiding by the Belmont Report
  • Regulatory framework and best practices
  • Protecting vulnerable populations
  • Problematic language to avoid
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Description

Recruitment materials are a potential participant’s first introduction to the study, and post-consent materials can influence an individual’s decision about continued participation. It is important to adhere to the principles of subject protection—that is, allowing subjects to make informed decisions about what is in their own best interest— with the materials that appear at the earliest stages of recruitment as well as through the life of the study.

Who should read?

Sponsors, CROs, research sites, and IRBs, along with PIs and study staff who are charged with creating and interpreting participant materials to ensure participants comprehend the details and expectations of a research study that they are considering joining.

Presented by Quorum

Quorum Review IRB is the first name in streamlined, service-centered independent ethics and regulatory review. The Quorum difference is One-Touch Collaboration™. Your research benefits from an outstanding service experience, a single point of contact, one study startup timeline, and a true single board review—which is why Quorum is the preferred central IRB. Beyond traditional institutional review board services, Quorum offerings include single IRB (sIRB) services for institutions and the world’s first IRB-integrated electronic informed consent solution: Q Consent™.