BrandLens uses 5 specialized AI experts to review your pharmaceutical marketing collateral against Indian regulatory guidelines (UCPMP, MCI, Drugs Act). Get comprehensive compliance analysis before your MLR team review.
BrandLens helps pharmaceutical marketing teams validate promotional materials before formal MLR (Medical, Legal, Regulatory) review — reducing revision cycles and accelerating time-to-market.
Checks against UCPMP 2024, MCI guidelines, Drugs & Magic Remedies Act, and FDA advertising rules specific to Indian pharma regulations.
Specialized AI reviewers for Compliance, Medical Claims, Visual Design, Copywriting Quality, and Industry Best Practices.
Upload backup documents, prescribing info, and clinical studies. AI validates claims against your actual reference materials.
Visual aids, detail aids, leave behinds, emailers, journal ads, patient brochures, conference posters, and more.
Get severity-graded findings with specific locations, recommendations, and downloadable PDF reports.
Upload your collateral and get comprehensive AI analysis in minutes. No more waiting for days.
Reviews regulatory compliance against UCPMP 2024, MCI Ethics Code, Schedule K, and Indian advertising regulations.
Validates scientific claims against backup documents, prescribing information, and PubMed literature.
Analyzes medical imagery accuracy, graph integrity, cultural appropriateness, and brand consistency.
Evaluates messaging clarity, audience appropriateness, and readability scores. Provides rewrite suggestions.
Checks industry standards for slide count, information flow, content density, and citation formatting.
Catch compliance issues before formal review, reducing back-and-forth with your MLR team.
Built specifically for Indian pharma marketing with UCPMP 2024, MCI, and local guidelines.
Upload your backup documents and let AI validate claims against your actual references.
Get specific findings with severity grades, locations, and recommendations in minutes.
Start using BrandLens today to streamline your pre-MLR review process.
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