eSource & Patient Engagement Symposium

Clinical trial Sponsors and CROs are transforming their clinical trials using Clinical Ink technology. See how these innovators are replacing EDC with advanced solutions that improve patient compliance and retention and simplify data collection in clinical trials.

Join us at the renowned Ninety Acres Culinary Center in Peapack, NJ on June 7 from 12 noon to 6:30 pm.   Limited Seats Available  >>

Imagine clinical trials where patients adhere to the protocol, and remain enrolled; where sites enter data the same day as the patient visit while reducing errors and queries; where monitors address risks, rather than SDV; where sponsors reduce costs and improve quality while also reducing timelines. It's here now. Without complex EMR integration.

It's time for a better Clinical Trial Experience - hear from your peers how they are getting there. 

12:00 - 1:15 pm. Seasonal lunch options available to all guests

1:30 - 5:15 pm. Guest Presentations

• eSource & Data Integrity: Thomas Haag, Learning and Process Lead - Digital Development, Novartis
• eSource 'All In': Maria Feldman, Vice President, Clinical Research and Operations, Regulatory Affairs and Quality Assurance, Neothetics
• Why Smart eSource will Revolutionize the Clinical Trial Industry: Dr. Leonard Chuck, Medical Director, Diablo Clinical Research
• "Please don't hang up,... .can you achieve rapid deployment of ePRO on BYOD in 3 weeks?": Michelle Hylan, Clinical Operations Consultant, Rhythm Therapeutics - Founder & CEO, Innov8tive Research Consulting
• eSource as a Foundation for Risk-Based Monitoring: Courtney McBean - MDD Consulting