Implementing the New Common Rule—Practical Advice for Research Organizations

A free on-demand webinar to help your organization prepare for the new Common Rule, effective January 21, 2019

This free webinar will explore the actual implications for institutions, health systems, and research organizations. After the webinar, attendees will know the crucial decisions they need to make when implementing the key elements of the new Common Rule:

  • Application of the Rule in your organization
  • Jurisdiction over independent IRBs
  • Informed consent requirements
  • Broad consent
  • Continuing review
  • Exemption determinations
  • Limited IRB review

Watch the webinar

Who should watch

Institutional Officials, VPs of Clinical Operations, IRB Directors, IRB Chairs, Principal Investigators, Study Coordinators and Clinical Research Associates at study sites, institutions and health systems organizations. Also, members of these organizations who are charged with implementing the new Common Rule.


James Riddle, MCSE, CIP, CPIA

James RiddleJames is VP of Client Services at Kinetiq. He previously worked as Assistant Director at the Fred Hutchinson Cancer Research Center and has over 15 years of experience leading private and academic human subject protection programs. He has been a site visitor for AAHRPP, is a faculty member, mentor, and regular speaker for Public Responsibility in Medicine and Research. James served on the Board of the Northwest Association for Biomedical Research, and is a Certified IRB and IACUC Professional.

Mitchell E. Parrish, JD, RAC, CIP

Mitchell ParrishMitchell is VP of Regulatory Affairs at Kinetiq. He has served in-house and outside counsel roles as a consultant to the National Cancer Institute, as a regulatory counsel to a large central IRB, and as an associate attorney at the global law firm K&L Gates. He is a frequent speaker and published author on clinical trials topics. He is a member of the Washington and Oregon State bars and Regulatory Affairs Professionals Society; is a Certified IRB Professional (CIP); and has his Regulatory Affairs Certification (RAC).



Continuing Education Credits
This webinar is pre-approved for 1.0 contact hours of continuing education credit for the Certified IRB Professional (CIP) certification, and for Maintenance of ACRP’s CCRC®, CCRA®, CCTI® or CPI® certifications. If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements. Information for CE credits for SOCRA can be found here. Visit our Webinars Help page for more information on certification credits.

Certificate of Attendance
You must watch this webinar in its entirety to receive a certificate of attendance. The certificate will include your full name and it will be emailed to you at the end of the webinar. Please note that if your organization has other staff members who wish to earn CE credits for this webinar, each person must register for and watch the webinar in its entirety in order to receive a certificate. Visit our Webinars Help page for more information on certificates of attendance.

Register to Watch Now: Implementing the New Common Rule—Practical Advice for Research Organizations

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