Join our team of experts for two sessions:

IQVIA Session 1: DCT Technology Due Diligence:  Sponsor Obligations for DCT Technologies and How to Meet Them

May 4, 3:15 pm, Outsourcing & ClinOps
Owen Corbin JD CIPM, Senior Director, DCT Regulatory and Data Privacy

Clinical trial regulations make sponsors responsible for the conduct of decentralized clinical trials (DCT) in accordance with GCP, as well as other laws and regulations. This responsibility extends to technology deployed in the conduct of DCT. In this session, sponsors will learn about:

• GCP, privacy and clinical trial requirements to consider when selecting and configuring technology products
• Common challenges in conducting due diligence in DCT technologies
• Suggested approaches for evaluating DCT technologies

IQVIA Session 2: Discover how IQVIA's Integrated IRT eCOA solution improves data quality and usability while simplifying and accelerating study design and conduct.

May 5, 3:00 pm, Plenary
Kevin Landells, VP, Project Management & Head of Global Project Management and Helpdesk.

• Establishing an architecture that imbeds the right business logic into your API's and reporting strategies through sponsor/vendor collaboration
• Ensuring data quality and availability through the timely exchange of the right data, and building reports that matter
• Looking beyond data exchange to opportunities to automate workflows, eliminate redundant tasks and improve oversight
• Enabling faster decision making which improves data accuracy and patient compliance by simplifying the site experience