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Description
There have been stunning scientific advances in
human stem cell-related research that abut an array of ethical and regulatory
issues. To help address these issues at a practical level, the International
Society for Stem Cell Research (ISSCR) updated its guidelines, which were
released in May 2021. This session, which includes bioethics members of the
global task force that updated the guidelines, will guide attendees through
important IRB-specific aspects of the revised ISSCR guidelines. Speakers will
provide an overview of the guidelines and discuss areas of human stem
cell-related research that merit IRB review, including the procurement of
biospecimens used to derive new stem cell lines, unique considerations for
clinical translational research, and the differences between IRB review and the
ISSCR’s specialized oversight system for stem cell research.
This webinar is based on a session the speakers presented at the 2021 AER Conference.
Agenda
- The Development of Guidelines for Human Stem Cell Research/Overview of New Guidelines
- Laboratory Based Research, Specialized Oversight Processes and the Procurement of Biospecimens
- Guidelines for Clinical Translation
- Q&A
- Discuss the relationship of the ISSCR Guidelines to existing mechanisms of ethics oversight such as IRBs.
- Understand the special considerations for IRB review for stem cell related research (such as that involving biospecimens and clinical translation).
- Identify research that warrants specialized oversight that falls outside the remit of IRBs.
IRB members, chairs and staff; Institutional Officials: researchers; IACUC and ESCRO members, chairs and staff. No prerequisite knowledge is required.
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To receive complimentary registrations, first register the paid registrants (e.g. if you’re using the buy 4 get 1 free discount, register the 4 paid individuals first) and then email onlinelearning@primr.org with a list of those paid individuals, as well as the name(s) and emails of those to receive complimentary registration.
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Access Interval
Access to live content will be available for 90 days after the recording is made available. After 90 days, access to the content will be removed, but users will retain access to any certificates of attendance earned. To earn a certificate, one must complete all required sections and complete the certificate section within the 90-day access period. After access has expired, users can purchase an additional 90 days of access.
If you prefer, you can find a paper registration form here. Please send the completed form to registration@primr.org.
Continuing Education
Webinar participants holding the Certified IRB Professional (CIP®) credential may apply 1.25 continuing education credits towards CIP recertification. Learn More
Thank you to our sponsor!
WCG IRB provides the highest quality ethical reviews of clinical research protocols and studies.
*Please note that you cannot purchase this webinar on behalf of others. If you would like to register a colleague or a group, please fill out the paper form or contact onlinelearning@primr.org for an invoice.