Date of Event: September 10, 2026

Location: Philadelphia, PA

Gain practical, regulatoryaligned strategies for meeting global clinical disclosure requirements, improving data transparency processes, and safeguarding sensitive information in an increasingly complex compliance landscape.

Topics to include:

  • Meeting global registry and regulatory disclosure requirements
  • Practical approaches to streamline operations
  • Integrating AI to accelerate and augment disclosure processes
  • Managing rising workload demands
  • Harmonizing the synergy between EU CTIS and ClinicalTrials.gov
  • Protecting data and commercially confidential information (CCI)
  • Updates on data anonymization techniques
  • Lessons learned from CTIS submissions and transitions under the EU CTR
  • Requirements and best practices for plain language summaries
  • Latest regulations and practices in broader clinical data sharing

More information to come