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Clinical Trial Application and Workload Management in CTIS
Session Chair(s)
Gabriella Di Matteo
CTRSE EUCTR Advocacy Lead & Strategic Execution, 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
ACT EU Programme Manager, European Medicines Agency, Netherlands
Tools for User Workload Overview and Management
Laura Pioppo, MSc
ACT EU Programme Manager, European Medicines Agency, Netherlands
Panel Discussion with Q&A and the additional participation of:
Kristof Bonnarens, MPharm
Policy Officer Pharmaceuticals, European Commission, Belgium
Panel Discussion with Q&A and the additional participation of:
Stéphanie Kromar
Senior Regulatory Affairs Manager, European Organisation for Research and Treatment of Cancer (EORTC) , Belgium
Ruediger Pankow, DRSc
Clinical Trial Regulatory Consultant | CTIS SME, Independent Consultant, Germany
Pieter Vankeerberghen
Head of Clinical Trials, European Medicines Agency, Netherlands
Future Master Trainer’s involvement and Current Status
Sara Torgal, MPharm
, European Medicines Agency (EMA), Netherlands
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