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A SPECIAL
ANNOUNCEMENT FROM:
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Just Announced: Keynote Speaker Donna R. Cryer, JD! Add noreply@DIAglobal.org.
 
 
Global Clinical Trial Disclosure and Data Transparency Conference
Are you familiar with these four regional clinical trial registration and transparency guidelines?

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.

Join DIA and an all-star lineup of speakers at DIA's Global Clinical Trial Disclosure and Data Transparency Conference, September 19-20 in Bethesda, MD to learn critical and timely information relating to global clinical trial disclosure and data transparency.
 
REGISTER AND SAVE
 
What's on the Agenda?
 
 
  Lf Border   Global Approaches of Data Sharing and ICMJE Data Sharing Requirements  
 
 
 
  Lf Border   Overview of Disclosure Requirements for Federally Funded Trials  
 
 
 
  Lf Border   Status and Latest News on the EU Regulatory Requirements Related to Disclosure of Clinical Data  
 
GET THE FULL AGENDA
 
Featured Speakers
 
 
  Lf Border   Donna R. Cryer, JD, Interim Executive Director, People-Centered Research Foundation, Keynote Speaker  
 
  Lf Border   Rebecca Williams, PharmD, MPH, Acting Director, ClinicalTrials.gov National Library of Medicine, NIH  
 
 
 
  Lf Border   Andre Molgat, PhD, Manager, Public Release of Clinical Information Health Canada, Canada  
 
 
 
  Lf Border   Pamela Miller, Assistant to the Editor, New England Journal of Medicine  
 
 
VIEW ALL SPEAKERS
 
Upcoming Trainings
 
 
  Lf Border   Navigating Chemistry, Manufacturing, and Controls Through the Drug Development Process | August 12-13  
 
 
  Lf Border   New Drug Product Development and Lifecycle Management |
August 12-13 		 
 
 
  Lf Border   Drug Safety and Pharmacovigilance Across the Product Lifecycle | August 12-14
  
 
 
  Lf Border   Regulatory Affairs: The IND, NDA, and Post-Marketing |
August 12-15 		 
 
 
  Lf Border   The Pharmacovigilance Quality Management System | August 15-16
  
 
 
VIEW AUGUST COURSES
 
 
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