Veeva R&D Summit US 2024

The increasingly complex and fast-moving clinical trial landscape has underscored a need for an agile and innovative Clinical Data Management Systems (CDMS). Top 20 pharmaceutical companies, emerging biopharma companies and leading CROs are moving toward modern cloud applications to build study databases faster, improve efficiency for study teams and drive greater consistency in data management. 

A case study performed by Syneos Health demonstrates that when implemented and delivered correctly, these systems can reduce end-to-end data management (DM) cycle times by up to 75%. 

Syneos Health is a certified Veeva Implementation Partner and have global experience supporting the implementation of ClinOps, CDMS, RIM and Quality Vaults. Our Consulting group partners with pharmaceutical sponsors to drive the business process engineering, OCM and training needed to guide the transformation journey - and prepare for impactful launch and adoption.

Meet with Us

Find Syneos Health at the Veeva R&D US Summit and schedule a meeting to learn how to transition to and implement Veeva Vault efficiently, ensuring your “business as usual” phase swiftly lays the foundation for delivery excellence. 

Related Content:

Want to learn more? Explore Insights Hub for our latest perspectives, subscribe to our podcast, or click the resources below:  

Veeva CDMS Implementation, Process Definition Support and Delivery Excellence 

DE&I Transformation in FSP Partnerships: Building the Clinical Trials Team of the Future 

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