CenterWatch Announces — The Basics of GDPR for Researchers, April 1, 2019

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Personal data… special categories of personal data… pseudonymization… What do they mean in GDPR speak?

WCG Market Intelligence & Insights

WCG Market Intelligence & Insights

The Basics of GDPR for Researchers
A MAGI/CenterWatch Free Webinar
Monday, April 1, 2019 · 1:30 p.m. – 2:30 p.m. EDT

Knowing the rules and applying the requirements of the General Data Protection Regulation (GDPR) to multi-national clinical trials and other research studies is necessary.

Mark the 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, attendees will:

  • 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.

The speakers are David Peloguin, Melissa Markey and Katherine Mahoney. David Peloquin practices law at Ropes & Gray LLP where he is a member of the firm’s health care group. Melissa Markey is a shareholder with Hall, Render, Killian, Heath & Lyman where her practice focuses on cybersecurity, privacy and life sciences issues. Katherine Mahoney is the Head of the Global Spend Transparency for the Global Medicines Development Affairs department at Vertex Pharmaceuticals where she ensures compliance with the GDPR.

Take part in this valuable free webinar to be well equipped when GDPR applies to a study.
Visit our website for registration and more information.

Webinar Details:
The Basics of GDPR for Researchers
A MAGI/CenterWatch Free Webinar
Monday, April 1, 2019 · 1:30 p.m. – 2:30 p.m. EDT

$287 per site

Easy Ways to Register:
By phone: 617-948-5100 or 866-219-3440

About CenterWatch:
Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.

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Michelle Butler
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