Luvia
Luvia is an AI research platform that applies reasoning across the complete, current record of a field—every trial, patent, and label for pharma and biotech, and every statute, case, and ruling for legal. Users can ask questions from any angle and trace every answer back to its source, with point-level citations such as ECLI and r.o. . The platform surfaces adverse evidence as readily as supporting findings, leaving judgment to the professional.
- Legal Technology
- Data & Analytics
- Artificial Intelligence
- Biotechnology
- Software Only
Funding
Founders
Founder details are not available yet.
Product
Problem
Professionals in pharma, biotech, and legal need to reason across vast, complex bodies of evidence—from clinical trials and patents to statutes and case law—but standard search tools return isolated results without connecting the full history of a drug or line of authority. Critical context, such as why a program failed or whether a precedent is still good law, is often buried across disparate documents, making thorough analysis time-consuming and prone to missing adverse evidence.
Solution
Luvia provides an AI research platform that applies reasoning across the entire, current record of a field, enabling users to ask questions and follow every answer back to its source. For pharma and biotech, the engine connects a drug's complete history—target, molecules, trials, patents, labels, and filings—to reveal why a program worked or failed, with every finding linked to its original document. For legal, it traces lines of authority from statutes through interpreting cases and higher court rulings, flagging whether a precedent is still good law, with each point pinned to its passage (ECLI, _r.o._). The system surfaces adverse evidence as readily as supporting evidence, leaving judgment to the professional rather than delivering an unverified opinion.
Target Audience
Primary users are research and analysis professionals in pharmaceutical companies, biotechnology firms, and legal practices who need comprehensive, source-verified answers across their field's complete record.
Features
- Unified reasoning engine across two source schemas—pharma/biotech and legal—in a single platform
- Cross-document entity linking for drugs (target, molecules, trials, patents, labels, filings) and legal authorities (statutes, cases, rulings)
- Point-level citation with source identifiers (including ECLI and _r.o._) for full traceability of every answer
- Explicit surfacing of adverse evidence and negative results alongside supporting findings
- Legal-specific functionality to determine whether a precedent remains good law after subsequent narrowing or overruling