Learn. Adjust. Implement.
The CTIS regulations alongside FDA regulations has given the clinical data disclosure and transparency landscape a renewed interest for professionals and requires a space for discussing best practices regarding global regulations going forward. This summit will explore how to quickly create experts in any sized organization on these clinical data disclosure policies and discover how to be confident in earlier disclosure of clinical trials.
Speakers

Riccardo Ferraiuolo

Faranak Jamali, M.D.

J.R. Meloro

Kathleen Ormiston

Oladayo Oyelola, PhD, SC(ASCP)

Sameer Sharma, MPharm

Adian Talib

Laura Troast

Who Should Attend

This event is developed for professionals from Pharmaceutical, Biotech, and Medical Device Companies with the following titles (Director to C-level):
- $Clinical Disclosure
- $Clinical Transparency
- $Clinical Registration
- $Regulatory Affairs
- $Clinical Operations
- $Data Privacy
- $Clinical Development
- $Medical Publications
- $Medical Writing
- $Medical Affairs
- $Clinical Pharmacology
- $Corporate Communications
- $Corporate Operations
- $Intellectual Property
- $Statistical Programming
- $Investor Relations
- $Epidemiology
- $Disclosure and Transparency Consultants
- $Transparency and Disclosure Cloud Platforms
- $Regulatory Services
- $Data Anonymization Services
- $CRO Pharma Solutions/Data Management Services
- $Healthcare Communication Solutions
- $Clinical Trial Disclosure Solutions
- $Medical Writing and Editing Consultants
Group Discount Available!
If you’re interested to learn more, please contact Arianne Leclair at
arianne@momentumevents.com
Key Takeaways





