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