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Overview
Narrativa builds generative artificial intelligence for regulated content, especially clinical trial documents. Its systems draft reports from structured study data. The company works with pharmaceutical and financial customers.
News
Oversight is only as strong as the evidence behind it
The EU AI Act requires more than human involvement in high-risk AI systems. Article 14 requires those responsible for oversight to remain aware of the risk of over-reliance on AI output and to be capable of disregarding, overriding or reversing it when ap
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Report
How to measure the ROI of regulatory AI in pharma
Artificial intelligence can shorten regulatory writing workflows, but speed alone does not prove value. Regulatory AI ROI (Return of Investment) must also account for review effort, quality, traceability, compliance, adoption, and capacity. This distincti
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Report
Narrativa and VMD Sciences bring agentic AI to veterinary regulatory documentation
Narrativa has partnered with VMD Sciences (VMDS) to implement an AI-driven solution for the automated generation of veterinary regulatory documents required for the compliant importation of global treatments across multiple countries and languages. This c
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Report
Valentina Soares joins Narrativa as Account & Operations Manager
We are excited to welcome Valentina Soares Gache to Narrativa as our new Account & Operations Manager. About Valentina Born and raised in Los Angeles with Argentine and Spanish roots, Valentina brings a unique international perspective and a strong track
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Report
What makes an AI system GxP-ready?
Introduction The rapid adoption of artificial intelligence (AI) in pharmaceutical operations is transforming how companies manage regulatory compliance. As AI technologies become more prevalent, ensuring that these systems are GxP-ready is essential. GxP
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Report
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Offices
Where the company hires and what each office is for
Cities
1
Hiring now
0
Countries
1
Madrid
Spain
HQ