Panel Site Partnering, Engagement & Operations track
PANEL DISCUSSION: We Mapped What Sites Actually Do to Prepare Source Docs—The Results Are Eye-Opening
Wed, Oct 14, 2026 · 11:15 AM–12:00 PM CEST InterContinental Barcelona
About this session
Sponsored by CRIO. Study start-up timelines have increased significantly. This session examines underlying causes including new data on how sites translate clinical trial protocols and information into template source documents and study support material. Tufts CSDD, in collaboration with CRIO, gathered survey data from 209 global investigative sites. Systems and workflows that sites use to capture, manage and transmit data and challenges encountered will be discussed along with opportunities to improve start-up efficiency, speed and quality.
Speakers
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Co-CEO, CRIO and Treasurer and Past Chair · Society for Clinical Data Management
Moderator
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Vice President, Head of Europe and Global Head of Franchises · Civia Health
Panelist
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MediVera
Panelist
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Executive Director and Professor, Tufts Center for the Study of Drug Development · Tufts University School of Medicine
Panelist
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