Medical Writing Pro

Equip your AI agent with medical & clinical writing expertise.

Install
cmdop skills install agensi-medical-writing-pro

Medical Writing Pro is a skill that adds domain-specific medical and scientific writing capability to a general-purpose AI agent. It targets the full publication lifecycle across four areas: journal submissions, congress deliverables, strategic planning, and quality control.

For journal submissions, the skill enables an agent to draft IMRaD sections, structured abstracts, and cover letters. For congress deliverables, it produces ASCO/ASH-compliant abstracts, poster narratives, and oral presentation scripts. On the strategic side, it supports gap analyses, journal selection, and publication planning. For QC and compliance, it executes AMA-style edits, MLR promotional language checks, and statistical reporting audits against CONSORT and STROBE guidelines.

The skill applies the ADAPT framework — Audience, Document, Accuracy, Purpose, Tone — to orient output toward its specific regulatory or academic context. It enforces data-anchored, non-promotional language and requires precise reporting of effect sizes with 95% confidence intervals and p-values. This directly addresses a common failure mode in general AI output, where vague or promotional phrasing fails Medical-Legal-Regulatory review.

This skill is appropriate for developers building agents for life-sciences companies, medical-affairs teams, or regulatory clients. It is not a general document editor and does not cover medical coding, adverse-event reporting, or regulatory submission formats outside of the publication context described above.

Use cases

  • Draft IMRaD manuscript sections for journal submission
  • Generate ASCO/ASH-compliant congress abstracts and poster narratives
  • Run MLR promotional language checks on clinical manuscript text
  • Audit statistical reporting against CONSORT or STROBE standards
  • Conduct journal selection and publication gap analysis
  • Apply AMA-style edits to clinical or scientific documents

When to use it

  • Building an agent for a pharmaceutical or medical-affairs team that produces publications
  • Automating MLR compliance review of promotional or clinical content
  • Generating congress abstracts or oral scripts that must meet ASCO/ASH formatting requirements
  • Enforcing non-promotional, data-anchored tone in scientific manuscripts
  • Supporting publication planning workflows for life-sciences clients

When not to use it

  • The task involves regulatory submission documents outside the publication lifecycle (e.g., CTD modules, IND/NDA filings)
  • Medical coding, pharmacovigilance, or adverse-event reporting is required
  • The agent needs to query or write to live databases — this skill has no tool integrations
  • General-purpose document editing or non-medical scientific writing is the primary need
  • A jurisdiction-specific compliance certification is required, as none is stated for this skill