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Clinical Trial Application and Workload Management in CTIS
Session Chair(s)
Gabriella Di Matteo
Director CTRO Team Manager
Pfizer, Belgium
This session navigates through the Clinical Trial Application Management step-by-step, folllowed by an overview on tools for user workload and how to manage. After an extensive panel discussion, an update on the current preparation for CTIS go-live is being shared as well as the future Master Trainer's involvement.
Speaker(s)
Clinical Trial Application Management Step by Step
Laura Pioppo, MSc
European Medicines Agency, Netherlands
Scientific Administrator, CTIS expert
Tools for User Workload Overview and Management
Laura Pioppo, MSc
European Medicines Agency, Netherlands
Scientific Administrator, CTIS expert
Panel Discussion with Q&A and the additional participation of:
Kristof Bonnarens, MPharm
European Commission, Belgium
Policy Officer Pharmaceuticals
Panel Discussion with Q&A and the additional participation of:
Stéphanie Kromar
European Organisation for Research and Treatment of Cancer (EORTC) , Belgium
Senior Regulatory Affairs Manager
Ruediger Pankow, DrSc
Germany
Regulatory Affairs Expert, CTIS SME and PO
Pieter Vankeerberghen
European Medicines Agency, Netherlands
Head of Clinical Trials
Future Master Trainer’s involvement and Current Status
Sara Torgal, MPharm
DIA, Switzerland
Senior Manager, Scientific Programs
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