HRPP Learning Library
HRPP Level: Beginner
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Create Recruitment Materials IRBs Love
Webinar slides provided by Quorum IRB on creating recruitment materials that are both compliant and compelling.
IRB Basics: Conducting Human Subjects Research at Brown (Video)
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 IRB Review Required?
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.
Herbie’s Research Pitfall Protections (HRPP): A Practical Guide to Submission Success
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.
Recruiting for Research Studies: Tips and Tricks for IRB Approval (Video)
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)
Undergraduate Research at Brown University
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).
Closing a Study: When and How to Manage Your Data (Video)
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
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Sponsor-Investigator (SI) FDA Inspections (April 2018)
Guidance on how to prepare for and what to expect from a Sponsor-Investigator FDA inspection.
IRB Authorization Agreements (IAAs) and Single IRB Review
Are you involved in or preparing for a multi-site research study? Be aware and prepared for IRB Authorization Agreements and Single IRB reviews.
We’re Engaged! Pro Tips for a Successful Collaboration (Video)
HRPP will walk you through the steps of determining engagement in collaborative research for realistic expectations for your study’s pending partnerships. (Slides)
Clinical Trial Compliance in the Era of the Revised Common Rule
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's That HIPAA in the Room?
What is HIPAA? This session will offer guidance and insight when HIPAA regulations apply to research.
International Research (Video)
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)