In today’s ACT Brief, we examine why the future of AI in trials is a trusted orchestration system rather than a single model, how coordinators rate eSource-enabled workflows, and what a bipartisan bill proposes for reusable trial networks.
|Articles|February 1, 2007
- Applied Clinical Trials-02-01-2007
- Volume 0
- Issue 0
eShowcase: Nextrials and Vitalograph
Partnership puts pulmonary data in the hands of researchers when and where they need it
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Partnership puts pulmonary data in the hands of researchers when and where they need it
Nextrials, Inc. (San Ramon, CA) is partnering with Vitalograph (Lenexa, KS, and Buckingham, UK) to deliver expedited access to pulmonary function data collected during clinical trials. The system works by closely integrating Nextrials' Prism clinical trial management system with the Vitalograph Spirotrac Centralized Spirometry System.
As a result, biotechnology and medical device researchers can quickly evaluate pulmonary lung function, potentially improving patient safety. For researchers, real-time access to study data also translates into enhanced workflow and efficiency. Ultimately, this results in reduced costs and quicker time to market for new therapies. As a result of the collaboration, sponsors have access to a single product that provides all relevant data including pulmonary function information, in real time across multiple test sites and multiple studies.
Nextrials, Inc., (925) 355-3000,
Vitalograph, (800) 255-6626,
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The Faster Clinical Trials Act would create an FDA Center for Clinical Trial Innovation and aims to cut trial costs and enrollment time by at least 30%.
Standardized measurement across five oncology centers found that clinical research coordinators rated eSource-enabled workflows positively (Overall Mean Satisfaction 5.79 of 7), with reduced manual entry and electronic data transfer earning strong marks, while perceived reduction in sponsor and monitor queries lagged as the one domain below threshold.
In this video interview, Rajneesh Patil, global head of AI, digital, and innovation in clinical development at Syneos Health, describes the industry’s trajectory toward a unified intelligence orchestration environment—and explains why the future isn’t one model that knows everything, but a trusted system that brings the right evidence to the right human decision.
In today’s ACT Brief, we examine how sites can avoid both fear-driven and overly aggressive AI adoption, why community-based research needs sustained financial investment, and why patient access matters more than organizational size.
Pacing obesity trial enrollment, anchoring eligibility to stable real-world therapies, and building site and physician relationships improve retention and data quality more than aggressive recruitment or restrictive exclusion criteria do.
In this video interview, Rajneesh Patil, global head of AI, digital, and innovation in clinical development at Syneos Health, argues that CROs must act as orchestrators rather than aggregators—and that the real test of any AI ecosystem is whether it reduces sponsor coordination burden or just hands it back to them.
Syneos Health and Optum outline a joint model for trial planning, recruitment and site access, with no financial terms or timelines disclosed.
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