Registration:
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Agenda and Topics:
Hear from Leaders of CDISC, E3C, CDISC English Speaking User Group (ESUG) and Clinical Research Sponsors and have Interactive Discussions on Exciting Topics:
- Use of Standards for CRFs and Protocols to streamline research and improve quality from end-to-end
- Development of standards for therapeutic areas (TA), including diabetes, asthma, TB, Alzheimer’s, Parkinson’s and more
- Coalition for Accelerating Standards and Therapies (CFAST) Initiative with TransCelerate and FDA
- CDISC and the Innovative Medicines Initiative (IMI)
- CDISC Shared Health and Research Electronic Library (SHARE)
- EMA Transparency Initiative, FDA Standards Strategy, CDISC interest by Global Regulators
- How to get involved in CDISC and TA Standards Development