Veeva MedTech Honored with MedTech Breakthrough’s “Best Clinical Efficiency Solution” Award

Veeva MedTech is committed to delivering technology and services that help the medtech industry streamline the entire product lifecycle. In clinical development, with the changes in regulations like EU MDR and the growing need for post-market clinical follow-up (PMCF) trials, having agile systems and processes is critical to ensure long-term growth for device and diagnostics companies.

With continued collaboration with companies like B. Braun, Exact Sciences, and Illumina, Veeva MedTech is increasingly a trusted partner to accelerate the shift to more connected and digital clinical trials. We’re incredibly proud to build on that momentum as MedTech Breakthrough’s winner of the Best Clinical Efficiency Solution award.

The award program honors outstanding health and medical technology products and companies. This year’s program attracted more than 3,900 nominations from over 15 countries. This milestone recognizes Veeva’s leadership in helping customers standardize, manage, and track clinical development.

According to James Johnson, managing director, MedTech Breakthrough, “The clinical landscape is evolving and there is increasing demand for real-world evidence and post-market data, and stringent global regulatory requirements are making clinical research more complex.”

“Veeva MedTech provides a platform that delivers on this need, scaling along with a company as they develop new products by allowing them to run trials end-to-end on a connected system that provides both visibility and control,” adds Johnson. “Congratulations to the entire Veeva MedTech team on winning ‘Best Clinical Efficiency Solution.’”

Veeva MedTech is dedicated to providing solutions for device and diagnostics companies to streamline clinical operations and data management to help accelerate studies and centralize processes. Using Veeva MedTech clinical solutions, companies report a 90% reduction in monitoring visit preparation time and 40% faster study start up time. These are significant improvements that can help get products to patients much quicker.

Medtech companies using advanced clinical applications can:

– Speed trial study times with technology driven process improvements from database builds to monitoring

– Achieve real-time inspection readiness for better decision-making and visibility into trial status and reporting

– Streamline clinical operations with a single source-of-truth across the trial master file, clinical trial management, and site payments with connected solutions

– Unify clinical data and operations to streamline processes and improve how sponsors, CROs, and sites collaborate throughout the clinical trial

To learn more about Veeva MedTech clinical solutions, register to attend the Veeva MedTech Summit May 31–June 2 in Minneapolis.