Thank you for being a part of the 2018 European Site Solutions Summit and for taking the survey. Your feedback is very important to us and your input will be used to drive future initiatives. You can download the slide decks for the presentations below by clicking on the titles.
The Patient’s Voice
Elizabeth Vroom, Director, Duchenne Parent Project (The Netherlands)
The Site Landscape: Benchmark Your Site
Diana Foster, PhD, VP, Strategy & Development, Society for Clinical Research Sites (USA)
Breakout Session I: EU General Data Protection Regulation: What It Means for Your Site
Lisa Montague Hieb, JD, CIPP/E, CIPM, Global Privacy & Data Protection Officer, Syneos Health (USA)
Breakout Session II: Brexit’s Impact on UK & EU Sites
Alastair Nicholson, Policy Development Lead, HRA Approval (UK)
Sheuli Porkess, MRCP, FFPM, Interim Executive Director Research, Medical & Innovation, The Association of the British Pharmaceutical Industry (UK)
Beyond Randomized Trials
Andrew Barker, Manager, Diabetes Industry Partnership Programmes, Medtronic (Switzerland)
Vivienne van de Walle, MD, PhD, CPI, Director & Owner, PT&R (The Netherlands)
Tom Van Paepegem, Clinical Operations Manager, Harmony Clinical Research (Belgium)
Gerda van Wijhe, MSc, Head of Clinical Programs, Global ELN Center of Excellence Clinical Research (The Netherlands)
Facilitator: Rick Ward, VP, Commercial Operations, Trifecta Clinical (USA)
TransCelerate’s Impact on Sites
Diane Driver, Head Outsourcing Contracts & Strategic Partnerships, UCB (UK)
Paul Duffy, Director Clinical Research UK & Ireland, MSD (UK)
Sylvia Eberhardt, Shared Investigator Platform & Investigator Registry Business Lead, Roche (Switzerland)
Denise Reyes, Program Director, Sites Subcommittee, TransCelerate BioPharma Inc. (USA)