概要
Short Courses: September 18
Conference: September 19-20
Clinical trial information transparency is taking on new dimensions. Clinical trial sponsors and academia are facing a host of new registration requirements in the US, EU, and elsewhere. With evolving requirements comes new challenges, creating additional opportunities for knowledge-sharing and necessitating more interaction with peers. This conference will provide critical and timely information relating to global clinical trial disclosure and data transparency from those on the front lines.
NEW! This year's conference will have an even greater global presence than ever!
Check out our 2019 Program!
On-Demand Webinar
EU Device Regulations – The European Database on Medical Devices (Eudamed)The EU’s 2017 passage of new medical device regulations presents substantial changes in how clinical trials of medical devices are disclosed in the EU, from protocol approval to the reporting of summary results. In 2020, Eudamed will provide the public with a comprehensive view of medical device research and approvals throughout the EU. This webinar will look at the new EU requirements and discuss how sponsors can approach meeting them.
Register today!
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プログラム委員会
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Robert Paarlberg, MS Principal
Paarlberg & Associates LLC, United States -
Suzanne Carlson, MA Consultant
ABSD Associates, LLC, United States -
Kelly Coulbourne, MS Director, Clinical Trial Transparency and Disclosure
Pfizer Inc, United States -
Patrick Fawcett Information Disclosure Administrator, Office of Research Protections
University of Pittsburgh, United States -
Merete Joergensen, MBA, MSc Clinical Disclosure and Transparency Expert
Merete-J Consulting, Denmark -
Francine Lane, MBA Senior Director of Product Management
Citeline, United States -
Nate Root, MSc Associate Director, Disclosure and Transparency
Ionis Pharmaceuticals, United States
