Medical & Pharma AI Compliance Pack — Write, Evidence-Grade & MLR-Clear Your Content Before Submission
Everything to take AI-assisted medical and pharma content from draft to submission-ready, compliantly. Write to medical and clinical standards, rank your evidence by source quality, and pass MLR / COI / AI-use compliance checks — the full pipeline for high-stakes regulated content where a wrong claim or a missing disclosure is expensive. Save about 20% versus buying the skills separately.
You save $9 vs buying individually.
What's included (3 skills)
Give your agent CMPP-certified medical-writing expertise — 30+ frameworks for clinical manuscripts, congress content, and regulatory QC. Build compliant pharma/biotech workflows that pass MLR and peer review.
Audit AI-assisted medical and pharma content for compliance-readiness before it enters formal MLR review or journal submission. It checks claim substantiation and on-label scope, reference integrity (the acute AI risk: fabricated or misrepresented citations), fair balance and safety, AI-use disclosure, ICMJE authorship and GPP, COI and funding, data integrity and patient privacy, and adverse-event flags — then returns a PASS / REVISE / BLOCK verdict with the must-fix list. A readiness pre-check built for the regulated reality of medical communications — not a replacement for formal review.
A reusable rubric that grades every source by type, recency, authority, independence, and corroboration, then ranks them and resolves conflicts by evidence weight.