Is GDPR a Four Letter Word? Demystifying the EU data privacy law and its impact on research
Join us on March 19 or March 21, 2019 at 10 AM (PST)/ 1 PM (EST)
This free webinar will explore how GDPR data privacy regulations do not just apply to research-related organizations in the EU. The data protections cover all entities if they process personal data—not merely participant research data—that originates within the EU. Join this webinar to understand the regulatory impact of GDPR for your organization—including governance of data processing and sharing, data subject notice and informed consent, and interplay with US regulations. It will be crucial in contouring your research roadmap and operations more broadly to ensure compliance.
- Outline EU GDPR scope, key definitions and requirements, and regulatory impact on researchers and research organizations
- Evaluate operational implications of GDPR regarding protection parameters around informed consent, future research, research transparency, data processing and sharing, data transfer outside the EU, as well as business privacy policies and responsibilities
- Highlight GDPR requirements in contrast to US data privacy, security, and confidentiality regulations
- Offer potential solutions for updating policies, procedures, and practice for compliance with GDPR
Who should watch
Content applies to roles at Study Sponsors, CROs, Institutions, and Research Sites, including: Research executives, managers, coordinators, IRB chairs, managers & administrators; legal counsel executives and privacy/compliance professionals; and principal investigators
Aarthi B. Iyer, JD, MPH, CIP
Aarthi previously worked in the health services research sector for major institutions and initiatives, including Harvard Pilgrim Healthcare and the FDA Sentinel System, Aarthi provides regulatory guidance related to human subject protections. She has in-depth experience in the ethical review of clinical trials and public health activities and is a frequent speaker and author on health care research topics.
David C. Babaian, JD, LL.M, CIP
Served as Regulatory Attorney for Quorum Review IRB. Through his work in several positions he has developed expertise in health law, project management, and regulatory compliance. In addition to providing IRB education with NWABR and participating in working groups with CTTI, he has worked as a research assistant and laboratory manager at MD Anderson Cancer Center and as a judicial clerk with the U.S. Court of Appeals.
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.
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Tags: ceu credits, clinical research, Common Rule 2018, continuing education certification, continuing education credits, educational webinar, Independent IRB, IRB, Kinetiq, New Common Rule, on-demand webinar, Quorum Review, Quorum Review IRB, research, webinar