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Case studies, news and insights on AI for regulated documents across life sciences.

Case Studies

Real pilots from pharma and biotech teams, with measured results: hours saved, cost savings and expert-rated accuracy.

Featured customer story

Sanai AI pilot at a top-20 biopharma: 54,120 hours saved a year in R&D

A top-20 biopharma piloted Sanai's Automated Authoring and Query Engine across Process Development and R&D. Its own experts scored the Query Engine 94%, against 60% for a $10M+ internal tool.

View the Case Study
54,120
Hours saved a year across the Query Engine and Automated Authoring
$5.1M
Baseline annual savings for 150 seats
94%
Expert pass rate for the Query Engine, against 60% for a $10M+ internal tool
90%
Reduction in document drafting time

News & Insights

News, research and perspectives from the Sanai team.

Press release

Kymanox launches AI-enabled quality and regulatory capabilities, with Sanai

Kymanox's new Human Factors AI offering runs on Sanai's platform, customized and deployed for Kymanox. It automates the aggregation, review and summarization of human factors study data for combination products and medical devices.

Read on Kymanox.com
Kymanox
“Initially deployed within Top-20 pharma, our platform was built to meet the highest levels of compliance, and we are proud to bring that same standard of excellence to Kymanox and the clients they serve.”
John Walters, CEO of Sanai

Press

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