Free Webinar Series: An Educational Outreach for the Clinical Research Community
IRB Services is a service-driven organization demonstrating excellence in human research participant protection. We are committed to providing efficient customer-oriented services to research sponsors while at the same time providing the highest standard of human subject protection. We effectively partner with Sponsors, CROs, and Researchers to promote and deliver scientifically and ethically sound human research. We act to cultivate a culture of conscience both within our organization and all organizations with which we interact.
A key component of our mission is to actively participate in educational outreach initiatives to provide the clinical research community and it’s stakeholders relevant and current information on new regulations, government initiatives, industry trends, and new ideas not only to inform but also to challenge and facilitate new dialogue.
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•Gain Access to the thoughts of Key Opinion Leaders
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•Learn about the latest government initiatives from those actually involved in their formation
• Get updates on the latest regulations and their interpretation from industry experts
Upcoming webinars, Register Now!
Check back soon for new session announcements coming in second quarter of 2013.
Archived webinars now available on-demand:
Protection of Phase 1 Research Volunteers in an Age of Pandemics and Re-emergence of Contagious Diseases Long Thought Conquered, e.g., TB
Original air date: Friday, January 18, 2013, 1:00pm – 2:30pm EDT
Keynote speakers: Dr. Agnes Klein, MD, MPH: HEALTH CANADA
Director, Centre for the Evaluation of Radiopharmaceuticals and
Biotherapeutic Products in the Biologics and Genetic Therapies
Directorate
Dr. Richard Larouche, BPharm, MD: Pharmanet/i3
Director, Medical Affairs, Early Stage Development
A Risk-Based Approach to Monitoring - Implications for Sponsors, CROs, Investigators and IRBs — AN UPDATE
Original air date: Thursday, September 6, 2012, 1pm – 2:30pm EDT
Keynote speakers: Mr. Gary Yingling, BS, MS, JD, Partner, K&L Gates, Washington DC
Nicholas Alp, PhD, BM BCh, FRCP, DM, Vice President, Scientific Council,
ICON plc, and Hon. Consultant Cardiologist, Oxford
University Hospitals NHS Trust
Anick Duchesne, BSc, DSA, Senior Director, CRA Management - North
America, ICON plc
New FDA Guidance for Industry:
Oversight of Clinical Investigations - A Risk-Based Approach to Monitoring - Implications for Sponsors, CROs, Investigators and IRBs
Original air date: Tuesday, May 1, 2012, 1pm-2:30pm EST
Keynote speakers: Jack Corman, President, IRB SERVICES
Nestor Nituch, Director Clinical Operations, Bristol-Myers Squibb (retired)
Terri Hinkley, Director Clinical Operations, Helix BioPharma
Ronald Fehst, President, Ronald Fehst Research Consultants
Human Research Subject Protection: A Time of Reflection, Renewal and Reform? No--It’s time to Redesign!
Original air date: Monday, December 12, 2011, 1pm-2:30pm EST
Keynote speaker: Dr. Greg Koski, PhD, MD
Senior Scientist, James Mongan Institute for Health Policy
Associate Professor of Anesthesia, Harvard Medical School
Associate Editor, Journal for Empirical Research on Human Research Ethics
Former Director of OHRP
For more information or questions please contact us.
