Webinars
View previously recorded webinars hosted by BRANY. Access expert insights and best practices in regulatory compliance, research operations, and ethical oversight.
FDA Guidance on Safety Reporting: Key Changes and Takeaways
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SPeakerS
Raffaella Hart, MS, CIP
Sr. Vice President, IRB, IBC, and QA
Lauren Hartsmith, JD, CIP
Senior Vice President, IRB, IBC, and QA
Staying Audit-Ready:
Practical Compliance Insights for Clinical Research Sites
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SPeaker
Leah B. Persky, MS, CCRC
Clinical Research Compliance Auditor, BRANY
Ensuring Compliance in Gene Therapy Trials for Neurological Disorders: IRB and IBC Perspective
Gain a deeper understanding of how to ethically navigate gene therapy trials for neurological disorders, the regulatory challenges involved, the collaborative roles of the IRB and IBC, and best practices for consent capacity and legally authorized representatives.
SPeakerS
Raffaella Hart, MS, CIP
Senior Vice President, IRB, IBC, and QA
Linda Reuter, MS, CIP
Sr. IRB Director, BRANY
Venessa Rodriguez, CIP
IRB and IBC Superviser, BRANY
Thos Cochrane, MD, MBA
Director, Fellowship in Bioethics, Harvard Medical School
