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Virtual Event

2020 年 11 月 18 日 1:45 下午 - 2020 年 11 月 19 日 7:00 下午

(Central European Time)

4051 Basel, Switzerland

Clinical Trial Regulation Conference

Session 4: 1 Year Countdown: Are You Ready? Sponsors preparedness for CTR including non-commercials sponsors

Session Chair(s)

Rose-Marie  Swallow

Rose-Marie Swallow

Senior Manager, Policy & Research, Bayer Plc., United Kingdom

This session will present the thoughts of three Sponsor Product Owners who are working with EMA and the IT Developers preparing CTIS for audit and then go-live on: how things are proceeding, what practicalities Sponsors of all types and sizes might need to consider in this final countdown stage; and what tips and pitfalls they might want to consider when preparing for the implementation of the CTR in late 2021.

Speaker(s)

Ruediger  Pankow, DRSc

Ruediger Pankow, DRSc

Clinical Trial Regulatory Consultant | CTIS SME, Independent Consultant, Germany

Practicalities of using CTIS in the Future

Andrea  Seidel-Glaetzer, MA, RN

Andrea Seidel-Glaetzer, MA, RN

Head of Project Management , Coordination Centre For Clinical Trials Heidelberg (KKS), Germany

Operational Considerations of an Academic Institution or a Small Sponsor

Pierre-Frederic  Omnes, MPharm

Pierre-Frederic Omnes, MPharm

Executive Director, Life Sciences, TransPerfect, France

Operational Considerations of Large Organisation

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