Bryanston Street , London, W1H 7EH, United Kingdom
EU Clinical Trials Regulation: Anticipating the Changes
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Overview
This pre-conference short course will bring you up-to-date with current developments and preparations for the implementation of the new clinical trial regulation so far. The course will complement the knowledge and information you’ll receive within the following conference days. It is recommended to take part if you did not attend last year’s clinical trial regulation conference.
Featured topics
Workshop Chair:
Sini Eskola,Director Regulatory Affairs, EFPIA
12:00 Registration
13:00 Introduction including Roadmap for EU CTR implementation
Sini Eskola,Director Regulatory Affairs, EFPIA
13:30 EU CTR: preparing the organisation for change - a Sponsor perspective
Adam Smith, Development Excellence Leader; Roche, Switzerland
14:45 EU CTR: preparing for change - a CRO perspective
John Poland, Association of Clinical Research Organizations, UK
15:30 Refreshment Break
16:00 EFPIA CTiMonitor
Sini Eskola,Director Regulatory Affairs, EFPIA
16:40 VHP as a stepping stone to CT Reg: Sponsor perspective
Claire Berry, Roche, Switzerland
17:20 Wrap Up
Sini Eskola,Director Regulatory Affairs, EFPIA
17:30 End of the Workshop
Learning objectives
You will be up to date on current preparations for the implementation of the new clinical trial regulation
Understand the top line implementation challenges faced by sponsors, CROs, and member states