Virtual Event

2020 年 09 月 21 日 1:00 下午 - 2020 年 09 月 21 日 5:30 下午

(Central Europe Standard Time)

4051 Basel, Switzerland

EMA Clinical Trial Information System Webinar: Dynamic Demo of Sponsor Workspace

Clinical Trial Application and Workload Management in CTIS

Session Chair(s)

Gabriella  Di Matteo

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)

Laura  Pioppo, MSc

Clinical Trial Application Management Step by Step

Laura Pioppo, MSc

European Medicines Agency, Netherlands

Scientific Administrator, CTIS expert

Laura  Pioppo, MSc

Tools for User Workload Overview and Management

Laura Pioppo, MSc

European Medicines Agency, Netherlands

Scientific Administrator, CTIS expert

Kristof  Bonnarens, MPharm

Panel Discussion with Q&A and the additional participation of:

Kristof Bonnarens, MPharm

European Commission, Belgium

Policy Officer Pharmaceuticals

Stéphanie   Kromar

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

Ruediger Pankow, DrSc

Independent Consultant, Germany

Clinical Trial Regulatory Consultant | CTIS SME

Pieter  Vankeerberghen

Pieter Vankeerberghen

European Medicines Agency, Netherlands

Head of Clinical Trials

Sara  Torgal, MPharm

Future Master Trainer’s involvement and Current Status

Sara Torgal, MPharm

DIA, Switzerland

Senior Manager, Scientific Programs

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