Event recap

CDISC & TMF US Interchange

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Key takeaways and insights

Two full days at the CDISC & TMF Interchange delivered engaging presentations, demonstrations, and roundtable discussions across five tracks — keeping attendees at the forefront of the latest developments in CDISC and TMF standards and innovations. We were glad to connect with attendees alongside the Cencora TMF Solutions team and to contribute through several Cencora-led presentations.

In today’s increasingly complex clinical research landscape, CDISC provides critical clarity by enabling the accessibility, interoperability, and reusability of data — so information can translate into real impact for clinical research and global health. CDISC’s global community brings the vision and expertise, and together we strengthen the foundation that helps amplify data’s value and drive more meaningful clinical research.

With team across North America, Europe, and Asia-Pacific region, we blend global reach with local expertise

3,000
Consultants worldwide
30+
Global markets covered
235+
Brands represented

Helping breakthroughs break through
 

At Cencora, we’re leading the way to a place where your life-changing therapies can soar to impossible heights. Together, let’s create healthier futures for more patients around the globe.
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How to turn poor TMF quality into TMF operational excellence

Join Rob Jones, Product Manager for the TMF Practice Area. Learn actionable strategies and expert insights on how industry-leading organizations are building and sustaining robust Trial Master Files – bucking the widespread trend of substandard TMF quality that creates unnecessary risks and delays in trial execution and regulatory submissions.

We'll explore proven methodologies from TMF teams spanning small biotech startups to large pharmaceutical enterprises. These organizations have successfully implemented tools and workflows that ensure TMF completeness, quality, and timeliness, even when working with limited resources.

TMF Solutions

Cencora's comprehensive TMF solution suite helps ensure your Trial Master File remains inspection-ready while enabling your internal teams to focus on advancing clinical trials.  

Connect with our team

Our team of leading value experts is dedicated to transforming evidence, policy insights, and market intelligence into effective global market access strategies. Let us help you navigate today’s complex healthcare landscape with confidence. Reach out to discover how we can support your goals.