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Making Clinical Trial Information Accessible: Experiences in Developing Informed Consent Forms and Lay Summaries of Study Results
Session Chair(s)
D.K.Theo Raynor, PHD, MPHARM
Professor of Pharmacy Practice, University of Leeds, United Kingdom
Thomas Schindler, PHD
Director Global Regulatory Affairs - Regulatory Operations, BioNTech SE, Germany
Making Clinical Trial Information Accessible: Experiences in Developing Informed Consent Forms and Lay Summaries of Study Results
Speaker(s)
D.K.Theo Raynor, PHD, MPHARM
Professor of Pharmacy Practice, University of Leeds, United Kingdom
Applying User Involvement and User Testing to Improved Consent Forms - The Process and Findings
Jan Lynge, DRSC
Manager, Novo Nordisk A/S, Denmark
Developing a Company-Wide Strategy for Improving and Implementing
Kamila Sroka-Saidi, PHD
Senior Medical Writer, Boehringer Ingelheim GmbH and Co. KG, Germany
Challenges and Solutions in the Writing of Lay Summaries of Study Results
Thomas Schindler, PHD
Director Global Regulatory Affairs - Regulatory Operations, BioNTech SE, Germany
Company-Wide Implementation of a Lay Summary Process – Do’s and Don’ts
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