MedContent automates claim verification, source discovery, and annotation for pharmaceutical marketing materials.
Request Access to TrialJoin leading agencies already streamlining their MLR workflow
Editorial teams spend nearly half their time hunting through PubMed, prescribing info, and clinical trials to find supporting evidence.
Materials bounce between writers, editors, and MLR reviewers multiple times due to missing sources and unclear annotations.
Agencies outsource tedious annotation work, adding cost and turnaround time to every project.
MedContent handles the tedious work so your team can focus on what matters: creating compelling, compliant content.
Upload your draft and MedContent instantly identifies every factual claim that needs substantiation.
Search your reference library and find supporting evidence with confidence scores and direct quotes.
Catch problems before MLR review with automated risk scoring and suggested revisions.
Know exactly where every claim stands with a clear verification dashboard.
Drop in your PDF, PowerPoint, or Word doc along with your reference library.
MedContent identifies all factual claims that need substantiation.
Search your sources or let AI find supporting evidence for each claim.
Generate an annotated report ready for regulatory review.
Reduce annotation time from days to hours with automated source discovery and claim matching.
Catch unsupported claims and risky language before submission with proactive risk scoring.
Bring annotation work in-house with AI assistance that scales with your workload.
Join our early access program and be among the first to experience AI-powered fact-checking for pharma.
Request Access to TrialUse our APIs for claims identification, reference search, annotation, or risk scoring.