The following are the essential elements of the IRB process. Please read through and familiarize yourself with these elements before submitting a proposal; it will make the process quicker, easier and ...

Other documents to create early in the process include the data collection instruments. If you're new to this IRB process, ask someone to review your protocol before proceding to the other documents.

When preparing submissions for funding from NIH or one of the Common Rule Agencies, the following steps will help ensure a smooth IRB review process when UAB is the prime awardee of funding: Propose a ...

You can also call ORP at 617-552-4778 or email us at irb@bc.edu. ORP staff will be happy to help you navigate your way through the IRB process. If you are experiencing technical difficulties, please ...

SMART IRB is an IRB reliance model designed to streamline the IRB review process for multi-site studies, while ensuring a high level of protection for research participants. SMART IRB can be used for ...

Waivers are rare and granted only when specific requirements are met and documented by the IRB or HSRO. A successful consent process presents detailed information which is organized and presented in a ...

Please review the list of other study types that do not fit the IRB’s definition of human subjects research on the Application Process page. The removal of IRB review of classroom projects removes a ...

Human subjects research CITI training must be current for all study personnel before the review process can begin ... by the Office for Human Research Protections and Bowdoin College IRB Policy. It is ...

Human Subjects research proposals should be submitted through the ROAMWyo system. For any questions regarding the submission process or other IRB-related matters ...

Unless instructed otherwise, please make sure you have the following items to include with your application: consent/assent form (IRB Form 3.1) any written instruments, sample questions, and/or other ...

The goal of this policy is to enhance and streamline the IRB review process in the context of multi-site research so that research can proceed as effectively and expeditiously as possible. Eliminating ...