HRPP Learning Library
HRPP Level: Beginner
Webinar slides provided by Quorum IRB on creating recruitment materials that are both compliant and compelling.
Learn about Brown’s human subject research policies, forms and procedures. Demystify the submission and review process with tips to a speedy approval. (Slides)
Is it human subjects research? Is your study program evaluation? We discuss different types of research and how to determine if your study needs IRB review.
IRB submissions can be a maze-like jungle. Education! Forms! Data Security! Let Pitfall Herbie throw you a rope to leap safely toward IRB approval.
Want to recruit research participants but don't know where to start? Learn about the IRB's updated recruitment policy so your ads can be compliant and effective. (Slides)
Learn when and how to submit an Undergraduate Project Application with helpful tips from determining if your project needs review to examples of a good submission (Slides).
When is the right time and how do you close a study? What about data management and a retention schedule? This session will answer all these questions and more. (Slides)
HRPP Level: Intermediate
Guidance on how to prepare for and what to expect from a Sponsor-Investigator FDA inspection.
Are you involved in or preparing for a multi-site research study? Be aware and prepared for IRB Authorization Agreements and Single IRB reviews.
HRPP will walk you through the steps of determining engagement in collaborative research for realistic expectations for your study’s pending partnerships. (Slides)
Join us as we walk you through how to determine if your research is a clinical trial and compliance requirements under the revised Common Rule.
What is HIPAA? This session will offer guidance and insight when HIPAA regulations apply to research.
Are you planning on conducting international research? This session will provide an overview of the IRB policy and what information will be requested for submission. (Slides)