Transcription of Evolving Requirements For Posting Clinical Trial ...
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Oladayo Oyelola, PhD, SC (ASCP)Director, Clinical Trial Information DisclosureDaiichi Sankyo Pharma DevelopmentEdison, NJ 08837 Evolving Requirements For Posting Clinical Trial Information on the EudraCT and the EU Portal: Potential Impact on DemandCBI Clinical Data Disclosure and TransparencyPhiladelphia, PA. 18 & 19 January 20172 DisclaimerThe opinions expressed in this presentation are my own,and not that of Daiichi Sankyo presentation is for informational purposes are no representations or warranties expressed or implied, with respect to the usefulness or sufficiencyof the presentation for the purposes ofclinical Trial information EudraCT and EU Portal Requirements 3 Presentation Outline Background and Timelines of Clinical Trial Information D
Evolving Requirements For Posting Clinical ... • Applies to adult trials within EU and third countries, ... • Clinical trial overview & search ...
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Number 561 October 2017 Regulating Clinical Trials, Regulating Clinical Trials, Clinical trials, Search, EU Clinical Trials Register, European Union, Clinical, International standards for clinical trial, CenterWatch Drugs in Clinical Trials Database, Data protection, GCP Inspection of Ti Ml t FliTrial Master Files, EU Clinical Trials, Summary of Clinical Trial Results for Laypersons, GUIDE LINES O D B, Clinical Trials Regulation (EC) No, European Union Clinical Trials Regulation (EC) No