概要
The clinical trial processes will change dramatically in 2019 with the new portal and database - are you ready?
The new Clinical Trial Regulation will shake the business processes of both industry and regulators next year. What do you need to know to be ready from day 1? Our popular Clinical Trial Regulation Conference will:
- Inform on the implementation timelines, interpretation of the regulation by various countries and the European and national level changes
- Benchmark your organisation's progress against other key stakeholders within the sector
- Guide on direction to take with your internal system and process changes
- Give floor to EMA and CTFG to allow you to ask them directly about what is expected.
Make sure you're prepared - don't miss out on the hottest conference of the year.
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プログラム委員会
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Nick Sykes, MS Policy Advisor, Regulatory Strategy
EFPIA, Belgium -
Surendra Gokhale, DRSC, PHD Senior Director, Global Regulatory Affairs and Capability Development Lead
F. Hoffmann-La Roche Ltd, Switzerland -
Elke Stahl, PHD Senior Expert, Clinical Trials Department
Federal Institute For Drugs and Medical Devices (BfArM), Germany
