CDISC Interchanges are global events held annually on three continents with hundreds of attendees gathering to network, share their expertise, best practices, and lessons learned about implementing CDISC data standards.

Attend the Interchange to:

  1. Hear presentations and panel discussions from visionaries, thought leaders and global regulatory representatives on the latest trends and initiatives in clinical research
  2. Participate in the new CDISC Master Track for a deep-dive into the standards
  3. Discover regulatory expectations and tips for academic researchers in the preconference, Use of CDISC Standards in Academia Workshop
  4. Gain knowledge from case studies and best practices in standards implementation
  5. Stay up to date on new and upcoming CDISC standards 
  6. Discover the many benefits of the CDISC Library
  7. Network with colleagues, collaborators, and partners from around the globe and share expertise and ideas.

Who Should Attend?

Biostatisticians, Clinicians, Concept Modelers, CRF Designers, Data Managers, Decision Makers, Innovators, Medical Writers, Metadata Modelers, Programmers, Study Designers, Study Management, Team Leads

CDISC standards are required for regulatory submissions to the US FDA and Japan PMDA, recommended by the China NMPA, and requested for use by the European Innovative Medicines Initiative (IMI).