Virtual Event

2020 年 09 月 18 日 8:30 上午 - 2020 年 09 月 18 日 5:30 下午

(Central Europe Standard Time)

4051 Basel, Switzerland

Clinical Trial Regulation Information Day for CEE Countries

Session 5: Overview and Update on the Clinical Trial Information System (CTIS) in addition to the of EU Regulation Related Guidelines

Session Chair(s)

Mihaela  David

Mihaela David

Director Regulatory Affairs

PSI Pharma Support Romania SRL, Romania

Session 5: Overview and Update on the Clinical Trial Information System (CTIS) in addition to Overview of EU Regulation Related Guidelines

Speaker(s)

Fia  Westerholm, DVM, MSc

Overview and Update on the Clinical Trial Information System

Fia Westerholm, DVM, MSc

European Medicines Agency, Netherlands

Programme Assurance Manager

Steffen  Thirstrup, MD, PhD

Overview of EU Regulation Related Guidelines

Steffen Thirstrup, MD, PhD

European Medicines Agency, Netherlands

Chief Medical Officer

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