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Clinical Reports References

These references support local, deterministic drafting and review. They are not clinical, legal, regulatory, privacy, publication, or accreditation advice and do not establish compliance.

Safety boundary

File map

File Use
report_type_routing.md Select the artifact and exact source family before drafting
case_report_guidelines.md CARE case-report structure, consent, and publication safeguards
diagnostic_reports_standards.md Radiology, pathology, and laboratory field boundaries
clinical_trial_reporting.md CONSORT 2025, SPIRIT 2025, ICH E3, and ICH E6(R3)
safety_reporting.md ICH E2 and FDA safety-reporting distinctions
privacy_and_deidentification.md HHS de-identification methods and process limits
medical_terminology.md Versioned terminology and syntax-versus-semantics limits
data_presentation.md Aggregate tables, denominators, units, dates, and missingness
professional_review.md Ethics, accountability, review, and sign-off
sources.md Dated official-source ledger

Source handling

sources.md records primary or official sources checked on 2026-07-23. Requirements, regional adoption, controlled terminologies, and professional standards can change. Before real-world use, a qualified reviewer must verify the current official source, applicable jurisdiction, institution, sponsor procedure, protocol, statistical analysis plan, and target-journal instructions.

Terminology

“Required” in these references means required by the cited source within its stated scope, not universally required. “Complete” means structurally present in a manifest, not clinically correct. Script results never authorize use, release, signature, filing, or submission.