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