Just in Time GCP to Sponsor Veeva US R&D and Quality Summit 2026
We’re pleased to announce that Just in Time GCP will be a Gold Sponsor of Veeva US R&D and Quality Summit 2026, taking place October 20–21 in Boston.
Each year, Veeva US R&D and Quality Summit brings together life sciences professionals across clinical operations, clinical data, quality, regulatory, safety, research sites, and technology to exchange ideas, explore innovation, and learn how organizations are using Veeva solutions across R&D and quality.
We’re looking forward to being part of those conversations once again.
As both a Veeva Services Partner in Development Cloud and a Certified Veeva Basics Services Partner, Just in Time GCP combines Veeva expertise with a deep understanding of clinical operations, GCP, regulatory expectations, and inspection readiness. Our services focus on helping trial sponsors get more value from Veeva applications that support clinical operations and GCP quality processes.
Supporting Different Veeva Journeys
Organizations using Veeva Development Cloud and Veeva Basics have different needs, and our support reflects those differences.
Veeva Clinical and Veeva Quality Cloud
For sponsors using Veeva Clinical Operations and Veeva Quality Cloud, Just in Time GCP helps evaluate how existing capabilities support evolving clinical operations and GCP quality needs, identify opportunities to optimize functionality, and unlock more value from the technology they already have. Our support can continue as business needs, processes, and teams evolve.
Veeva Basics
For smaller and emerging biopharma organizations adopting Veeva Basics for clinical operations, our team provides business go-live support and clinical expertise to help sponsors adopt and operationalize the preconfigured solution and align their ways of working with its standardized processes.
Following go-live support, we help sponsors sustain adoption and effective day-to-day use as their processes and teams evolve, within the standardized Veeva Basics model.
In both cases, our focus is on bringing together technology and clinical expertise to support effective clinical operations, GCP compliance, and inspection readiness.
Revisiting the Value of Existing Veeva Capabilities
Regulatory expectations change. Business operations evolve. And the way organizations conduct and oversee clinical research continues to advance.
As those needs evolve, there is value in periodically taking a fresh look at how the technology already available to an organization supports the way it operates today.
That thinking inspired our new content series, Veeva Clinical and Veeva Quality Cloud Revisited: Perspectives from Just in Time GCP. The series explores selected capabilities in Veeva Clinical and Veeva Quality Cloud applications relevant to clinical operations, GCP quality processes, and inspection readiness, with a focus on getting more value from functionality already available.
Our first installment, Veeva eTMF Revisited, takes a fresh look at Risk-Based Quality Control and how existing Veeva eTMF functionality can support today’s increasingly risk-proportionate approach to quality and oversight.
As clinical research and trial management evolve, there is value in periodically looking at the technology that supports it with a fresh perspective.
Not because the technology needs to change.
Because the way we use it can continue to mature.
That is the inspiration behind Veeva Clinical and Veeva Quality Cloud Revisited, a new series from Just in Time GCP exploring existing Veeva capabilities through the lens of today’s clinical research environment.
Meet Us at Veeva Summit
If you’ll be attending Veeva US R&D and Quality Summit 2026, we’d love the opportunity to meet you.
Stop by our booth to talk with the Just in Time GCP team about your clinical operations and GCP quality needs, your Veeva journey, and opportunities to get more value from the Veeva applications you use.
We look forward to seeing you in Boston this October.
