How to Run Clinical Investigations in Greenlight Guru Clinical

January 14th, 9.00 AM ET (15:00 CET)

If you're currently managing clinical investigations with spreadsheets, manual workflows, or generic EDC tools, this session is for you. In this live webinar, Pall Johannesson will demonstrate how to practically plan and run studies inside Greenlight Guru Clinical, with a focus on simplifying execution while ensuring full compliance.

In this session, you will learn how to:

• Bring your EDC in-house with minimal operational burden, or effectively collaborate with CROs using permission-based access and flexible roles
• Align your studies to real clinical workflows at the site level using configurable visits, case-based data collection, and intuitive process design tools
• Navigate patient engagement using built-in ePRO and eConsent features, with secure subject authentication and automated reminders
• Ensure your study is built to support compliance with ISO 14155, FDA 21 CFR Part 11, and ICH GCP, including full audit trails, validation options, and electronic signature support

Whether you're planning a pre-market investigation or managing post-market clinical follow-up, this webinar will provide actionable insight into how Greenlight Guru Clinical helps sponsors:

• Accelerate study design and launch timelines
• Improve oversight and reduce dependence on CROs
• Collect higher quality data with less manual effort
• Operate with confidence in regulated environments