The Basics of GDPR for Researchers
Monday, April 1, 2019 · 1:30-2:30 pm EDT
Location: Your office or conference room (no need to travel!)
How does the European Union’s new privacy regulation impact your data? When does General Data Protection Regulation (GDPR) apply to your research study? What are your obligations?
Mark your calendar for a FREE webinar from three legal experts who will provide an overview of the key terminology used in the GDPR, the territorial scope of the regulation and the obligations it places on different parties in the research enterprise. Over the course of a fast-paced hour, you’ll:
- Understand the territorial scope of the GDPR
- Gain fluency with the key terminology used by GDPR, including terms like personal data, pseudonymization and anonymization
- Familiarize with the bases for processing personal data in clinical research
- Learn the key compliance obligations that the GDPR places on researchers — particularly those in the U.S.
Feel free to share this webinar invitation with others.
Who Will Benefit
- Privacy officers
- Study coordinators
- Principal investigators
Meet Your Presenters
David Peloguin, JD, Attorney, Ropes & Gray LLP
David Peloquin practices law at Ropes & Gray LLP where he is a member of the firm’s health care group. He focuses his practice on advising academic medical centers, life sciences companies, and information technology companies on issues related to human subjects and animal research, U.S. and European data privacy legislation as applied to the health care and research enterprises, and Medicare/Medicaid and other third-party payor reimbursement issues. He frequently writes and speaks on topics related to each of these areas.
Melissa Markey, JD, CISSP, EMT-P, Attorney, Hall, Render, Killian, Heath & Lyman
Melissa Markey is a shareholder with Hall, Render, Killian, Heath & Lyman. Melissa's practice focuses on cybersecurity, privacy and life sciences issues. She leads the Life Sciences team at Hall Render and has an interest in legal issues at the developing edge of technology. She is a nationally recognized author and presenter on data privacy and security, clinical research, research misconduct, and emergency preparedness and response law.
Katherine Mahoney, JD, Associate Director, Vendor Strategy & Management, Vertex Pharmaceuticals
Katherine Mahoney is the Head of the Global Spend Transparency for the Global Medicines Development Affairs department at Vertex Pharmaceuticals. She started her career managing start-up activities, including Clinical Trial Agreement and budget negotiation, drafting Informed Consent Forms, and gaining Ethics approvals. Since 2013, Katherine has acted as the Clinical Liaison to Corporate Compliance, and since 2017, Clinical Privacy Champion- ensuring that the clinical organization complies with the EU General Data Protection Regulation. Katherine has also taken a leading role in preparing the clinical organization for Brexit.