EMA Clinical Trial Information System (CTIS) Information Day

The focus of this live virtual CTIS information day is to share practical advice and best practices with regard to transitioning clinical trials, timelines in CTIS, system metrics, insights of clinical trial assessments as well as user management.

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Part II - Presentations

Session Chair(s)

Noemie Manent, PharmD

TDA-CTT Operations Workstream Lead

European Medicines Agency, Netherlands

Part II - Presentations

Speaker(s)

System Metrics on Ctis System Usage

Laura Pioppo, MSc

European Medicines Agency, Netherlands

Scientific Administrator, CTIS expert

Best Practices for Sponsor User Management

Gabriella Di Matteo

Pfizer, Belgium

Director CTRO Team Manager

Best Practices for Member State User Management

Marianne Lunzer, DrMed

AGES, Austria

Assessor, Dept of Clinical Trials, Federal Office for Safety in Health Care

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EMA Clinical Trial Information System (CTIS) Information Day

Part II - Presentations

Session Chair(s)

Noemie Manent, PharmD

Speaker(s)

System Metrics on Ctis System Usage

Best Practices for Sponsor User Management

Best Practices for Member State User Management

Be informed and stay engaged.