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Wednesday, June 27 • 9:15am - 9:45am
#322: New Resource from the DIA Interdisciplinary Disclosure Working Group

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Component Type: Session
Level: Intermediate
CE: IACET 0.50

Seating is limited
Clinical trial transparency requirements and initiatives have been changing the clinical trial disclosure landscape and affecting multiple functions within the pharmaceutical industry. Individuals within the pharmaceutical industry have held ongoing discussions identifying what is in scope for these requirements and finding ways to meet these regulatory requirements. Because these transparency regulations affect multiple stakeholders, a need for a group of professionals across functions to develop resources was needed. This session will highlight a resource developed by the DIA Interdisciplinary Disclosure Working Group for implementing clinical trial disclosures in the biopharma industry. This session will discuss the creation of this resource and how it may be used by professionals involved in clinical trial disclosure. (Submitted on behalf of the DIA Interdisciplinary Disclosure Working Group

Learning Objectives

Identify the challenges and opportunities in clinical trial transparency and disclosure; Discuss what skills and knowledge may be useful for those individuals involved in transparency and disclosure; Describe how the Interdisciplinary Working Group resource may be used by clinical trial disclosure stakeholders.


Eileen Girten, MS

avatar for Eileen Girten

Eileen Girten

Principal Medical Writer, PRA Health Sciences
Eileen M. Girten is a Principal Medical Writer with PRA Health Sciences and is experienced in regulatory and publications writing, submissions, and mentoring. She is an Adjunct Assistant Professor at the University of the Sciences in Philadelphia and has taught Regulatory Documentation... Read More →

Wednesday June 27, 2018 9:15am - 9:45am EDT
Content Hub NE Lobby Boston Convention and Exhibition Center 415 Summer Street, Boston, MA 02210 USA
  16: Content Hubs, Session