Evinova, a health tech company in the AstraZeneca group, uses Devin to draft regulatory documents for its clinical-trial software modules, work that took 35 to 40 hours of cross-functional time. Cognition reports structured first drafts at roughly 90% accuracy, with senior engineers shifting to reviewers.
Reported outcomes
Outcomes are reported exactly as stated by the source; we have not independently audited them.
How it works
- Devin assembles context from code and systems across teams.
- Produces structured first drafts of regulatory documents.
- Senior engineers review and approve.
Risks & compliance
- Regulated (GxP) software documentation requires qualified human review
- Vendor-published results
Healthcare cases cover operational and commercial workflows. Nothing here is medical advice or a claim about a device's or drug's efficacy.
Tools mentioned & how to build it
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Tools mentioned
- Devin (Cognition)
Autonomous AI software engineer from Cognition.
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Sources
“Devin produced structured first drafts at roughly 90% accuracy, shifting senior engineers from primary authors to reviewers”Evinova and Devin
Grade rationale: Named organization with a quantified outcome from the vendor or the organization itself (self-reported). Automated check on Oct 17, 2026: 1/1 quotes and 2/2 outcome claims matched the source. Compiled by the Agent Casefile research desk (AI-assisted; see methodology). Spot an error? Request a correction.
