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Part II - Presentations
Session Chair(s)
Noemie Manent, PHARMD
TDA-CTT Change Management Lead, European Medicines Agency, Netherlands
Part II - Presentations
Speaker(s)
Laura Pioppo, MSC
ACT EU Programme Manager, European Medicines Agency, Netherlands
System Metrics on Ctis System Usage
Gabriella Di Matteo
CTRSE EUCTR Advocacy Lead & Strategic Execution, Pfizer, Belgium
Best Practices for Sponsor User Management
Marianne Lunzer, DrMed
Assessor, Dept of Clinical Trials, Federal Office for Safety in Health Care, AGES, Austria
Best Practices for Member State User Management
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