2017 in Review – How Legal and Regulatory Changes Impact Your Research
A free on-demand webinar to help your organization
How are recent legal and regulatory changes fundamentally affecting clinical research? What is next?
In this complimentary webinar you will get answers to these questions and learn how research is impacted by:
- The 21st Century Cures Act
- FDA regulatory changes
- The new Common Rule
- NIH policy
- State laws
The speakers will explore what changes mean to your organization’s clinical research program and efforts to embrace new technologies. After this webinar, organizations will understand any practices to modify and policies to update.
Who should watch
Sponsors, CROs, Institutions, Sites and their research professionals including Institutional Officials, General Counsels, VPs of Clinical Operations, Compliance Officers, Regulatory Directors, IRB Directors, IRB Chairs, Principal Investigators, Study Coordinators and Clinical Research Associates. Also, members of these organizations who are charged with implementing the new laws and regulations.
Mitchell E. Parrish, JD, RAC, CIP
Mitchell is VP of Legal 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).
Dominic Chiarelli, JD, CIP
Dominic is the Manager of Legal Affairs at Kinetiq, where he ensures successful coordination of regulatory projects and development. He has served as a Regulatory Attorney at Quorum Review IRB and has in-depth knowledge of FDA, OHRP, and HIPAA laws and regulations. He has past experience as a regulatory analyst and IRB member for pediatric research, in addition to working as a research assistant for three major academic research centers in the U.S., Australia, and Spain.
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: 2017 in Review - How Legal and Regulatory Changes Impact Your Research
Tags: 21st Century Cures Act, ceu credits, CEUs, clinical research, Common Rule 2018, compliance, educational content, FDA, free webinar, IRB, legal, New Common Rule, NIH, OHRP, regualtory, regulatory consulting, research, webinar