May 18, 2026 · 4 min read
Medical Device Evidence Analysis in Hours, Not Weeks
Guanta built an AI-assisted clinical evidence workflow that helps medical device manufacturers search, screen, appraise, and document scientific literature for clinical evaluation.
- Client type
- Medical device manufacturer
- Industry
- MedTech / regulatory
- Outcome
- 30 days to about 4 hours
- reduced evidence review cycle time from weeks to hours
- less repetitive abstract screening and PDF handling
- more consistent literature review structure across devices