AI-assisted MLR review for pharma and biotech
Codi reviews pharmaceutical materials for compliance issues, claim substantiation and reference accuracy, giving your team precise, evidence-linked findings in minutes.
Works alongside your existing review process, including Veeva Vault PromoMats.
AI-assisted. Human judgement stays with your reviewers and signatories.
Codi × Indigo Medical
Combining pharmaceutical compliance expertise with Codi's AI technology.
Built for every role in the review process
Marketing
Catch avoidable compliance issues before material reaches MLR review.
Medical & reviewers
Spend less time on repetitive checks and more time on scientific judgement.
Compliance & signatories
Get consistent, traceable findings linked directly to Code provisions and source evidence.
What Codi checks
Mandatory compliance checks
Verify required elements are present and correctly positioned: brand name, INN, prescribing information including QR codes, declaration of involvement, MHRA Yellow Card wording, black triangle symbols, and customer-specific rules.
Claim substantiation
See whether a claim is supported by its cited source, with relevant supporting or contradictory evidence highlighted.
Reference validation
Check references for completeness and accessibility, and locate cited evidence quickly.
Visual compliance
AI vision analysis identifies potential visual compliance concerns in images and graphics.
Customer-specific rules
Configure and enforce your organisation's internal compliance requirements alongside ABPI checks.
Interactive findings
Ask questions using the ABPI Code, PMCPA precedent, and the material itself through an AI-assisted chat interface.
Fits the review workflow you already use
Add your material
Upload materials and supporting references.
Configure the review
Select the checks you want Codi to run.
Run checks in parallel
Compliance, claims, references and visual checks run together.
Review findings in context
See findings against the exact page, with severity and relevant Code references.
Investigate further with Codi
Ask questions using the ABPI Code, PMCPA precedent and the material itself.
Purpose-built for UK pharmaceutical compliance
Not generic document AI. Codi is designed specifically for ABPI Code compliance and MLR workflows.
Security and governance for regulated teams
Stored and processed in the EU
Customer materials and analysis results remain within EU hosting regions.
Tenant isolation
Enterprise deployments use isolated environments — no shared infrastructure or data between clients.
Your data is not used to train models
Documents and results are never used to train or improve centralised or third-party models.
Access control and auditability
Role-based access with persisted events and results for reviewable history.
See Codi review materials
See how Codi identifies ABPI issues, analyses claims and references, and gives reviewers evidence-linked findings in context.