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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
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
Programme Assurance Manager, European Medicines Agency, Netherlands
Overview and Update on the Clinical Trial Information System
Steffen Thirstrup, MD, PHD
Chief Medical Officer, European Medicines Agency, Netherlands
Overview of EU Regulation Related Guidelines
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