One of the primary responsibilities of the IRB administrator is to facilitate and streamline protocol review, in accordance with federal requirements for protecting human subjects. With the right tools, templates, and checklists, administrators can do so efficiently and in compliance with applicable regulatory requirements. (Presented on May 5, 2016)
Using examples from typically challenging areas of protocol review, the presenters will demonstrate how to identify, develop, and successfully implement targeted tools, templates, and checklists. Areas that were covered included:
- Screening of protocols upon receipt to determine submission completeness and the level of review required
- Facilitating IRB member reviews
- Using meeting minutes to document IRB determinations. [Consideration will be given to the new jointly released draft guidance from FDA and DHHS on IRB meeting minutes]
- Developing IRB correspondence to communicate IRB inquiries or determinations
What will I learn?
After attending this webinar, attendees were able to:
- Take advantage of tools, templates, and checklists to improve the protocol review process, and adapt pre-existing tools to fit their institution’s needs
- Understand the benefits and shortcomings of using checklists and templates in the IRB review process
Who should attend?
This intermediate-level webinar benefited IRB administrators who facilitate the review of biomedical and/or social, behavioral, and educational research (SBER) and wish to capitalize on the use of tools for developing systematic, defensible review processes at their institutions.
Continuing Education
Webinar participants holding the Certified IRB Professional (CIP®) credential may apply 1.5 continuing education credits towards CIP recertification. Learn More »
Access Interval
Access to purchased content will be available for 90 days after the date of purchase. After 90 days, access to the content will be removed, but users will retain access to any certificates of attendance earned. Content purchased prior to January 1, 2021 will remain available indefinitely. After access has expired, users can purchase an additional 90 days of access.
If you'd prefer a paper form, please click here. Please send the completed form to registration@primr.org.
Please note that this content is also part of a bundle. Click here to see the full bundle array.