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戻る Agenda
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)
Overview and Update on the Clinical Trial Information System
Fia Westerholm, DVM, MSc
European Medicines Agency, Netherlands
Programme Assurance Manager
Overview of EU Regulation Related Guidelines
Steffen Thirstrup, MD, PhD
European Medicines Agency, Netherlands
Chief Medical Officer