The company reports that its technology is already delivering measurable impact, including estimated cost savings of 5% to 7% per study. Those gains are largely driven by improvements in protocol design and reductions in downstream amendments.
Several core modules underpin the platform.
- Study Designer enables scenario-based protocol planning and benchmarking.
- AI Authoring supports the creation of clinical documents using structured data and prior learnings.
- AI Digitizer converts protocols and study materials into machine-readable formats aligned with Clinical Data Interchange Standards Consortium models, helping establish a reusable digital backbone.
“Transforming clinical development is not just an opportunity; it is an urgent necessity,” said Cristian Massacesi, MD, EVP, chief medical officer and head of development at Bristol Myers Squibb. “For years, developing medicines has taken too long, cost too much money, and mostly resulted in failure.”
Massacesi added that AI-driven tools offer a path toward more efficient development and better outcomes for patients, particularly as complexity continues to increase across therapeutic areas.
Evinova president Cristina Duran framed the collaborations as part of a broader shift toward AI-first operations.
“By uniting deep domain expertise with the power of AI, our strategic collaborations with life science leaders are moving the industry from heavy manual, fragmented processes to intelligent, AI-first workflows that deliver measurable benefits at scale,” she added.
The platform’s cloud-native architecture also allows organizations to integrate their own proprietary AI models, while maintaining data privacy and compliance across global markets.
Initial announcement of BMS partnership
Evinova initially announced its partnership with BMS earlier this month. As part of that agreement, Bristol Myers Squibb is deploying the Cost Optimizer module within Evinova’s Study Designer platform across its global development portfolio.2
The AI-enabled tool is designed to support more informed decision-making by identifying productivity opportunities and enabling more efficient study designs.
Evinova’s broader platform also incorporates agentic AI and standardized digital data flows aligned with USDM standards. According to the company, the system includes governance controls to support responsible AI use and has already been deployed at scale across multiple organizations.
Beyond protocol optimization, the platform connects various trial components—including electronic clinical outcome assessments, telehealth, and remote monitoring—into a unified digital environment.
The approach is intended to reduce operational friction for sponsors and sites while supporting more flexible trial models and improving data collection for emerging endpoints.
References
1. Evinova Announces Strategic Collaborations with Astellas, AstraZeneca and Bristol Myers Squibb Advancing Its AI-Native Platform to Accelerate Global Clinical Development. News release. Evinova. February 18, 2026. Accessed February 20, 2026. https://www.businesswire.com/news/home/20260218356317/en/Evinova-Announces-Strategic-Collaborations-with-Astellas-AstraZeneca-and-Bristol-Myers-Squibb-Advancing-Its-AI-Native-Platform-to-Accelerate-Global-Clinical-Development
2. Evinova, Bristol Myers Squibb Partner to Apply AI to Global Clinical Development. Applied Clinical Trials. February 10, 2026. Accessed February 20, 2026. https://www.appliedclinicaltrialsonline.com/view/evinova-bristol-myers-squibb-partner-ai-global-clinical-development