clinical-reports

# Clinical Reports ## Purpose Prepare **draft reporting structures**, aggregate tables, and review manifests from verified authorized facts. Route each artifact to the correct reporting guidance, preserve provenance, and stop when source support or qualified review is missing. This skill does not establish legal, regulatory, ethical, journal, accreditation, or institutional compliance. Its scripts check structure and internal consistency only. ## Non-Negotiable Boundary Never: - diagnose, recommend treatment, choose or change dosing, triage, or provide return precautions; - interpret images, specimens, raw laboratory results, symptoms, or other clinical observations; - invent, infer, normalize, “complete,” or silently reconcile observations, results, dates, units, denominators, causality, expectedness, seriousness, outcomes, or conclusions; - create an individual case safety report from patient-level narrative or decide reportability; - sign, attest, approve, file, transmit, submit, amend a source record, or act as a licensed clinician, pathologist, radiologist, laboratorian, safety physician, statistician, privacy officer, attorney, or regulatory professional; - use real PHI in examples, assets, tests, prompts, logs, or external services; - call an external LLM, image service, API, or another skill. All generated artifacts must remain visibly marked: > DRAFT — NOT FOR CLINICAL USE, SIGNATURE, FILING, OR SUBMISSION. Populate only from verified authorized source record...