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当用户需要对医疗险投保问卷进行专业、结构化的核保审查，提取既往症、门诊就医史、住院史、手术史、当前治疗、复查随访、近期检查异常和其他可能影响医疗险承保判断的高风险健康信息，并生成适合医疗险核保、补问流转和短中期风险分层处理的结构化分析结果时使用本 skill。
当用户需要对住院相关医疗资料进行专业、结构化的解析，提取入院诊断、出院诊断、住院经过、手术治疗、并发症、恢复情况、复诊建议及其他与核保相关的重要医学信息，并生成适合保险核保、补问流转和资料审查的结构化解析结果时使用本 skill。
当用户需要对门诊相关医疗记录进行专业、结构化的解析，提取主诉、现病史、初步诊断、复诊频次、治疗方案、随访安排及其他与保险核保相关的重要医学信息，并生成适合保险核保、补问流转和资料审查的结构化解析结果时使用本 skill。
当用户需要对常规体检报告进行专业、结构化的解析，提取异常指标、异常结论、边界值异常、复查建议、长期健康风险线索和与核保相关的重要医学信息，并生成适合保险核保、补问流转和资料审查的结构化解析结果时使用本 skill。
Cognitive framework for medical diagnostic decision-making addressing systematic biases (commission bias, satisfaction of search, availability error, anchoring error, attribution error). NOT for clinical knowledge acquisition or specific disease protocols.
当用户需要对与肿瘤相关的既往病史资料进行专业、结构化的审查，提取肿瘤类型、病理结果、分期分级、治疗经过、手术情况、放化疗或靶向治疗、复发转移风险、随访状态及其他与保险核保相关的重要健康信息，并生成适合核保审查、风险分层和资料流转的结构化分析结果时使用本 skill。
FDA MedTech Compliance Auditor workflow skill. Use this skill when the user needs Expert AI auditor for Medical Device (SaMD) compliance, IEC 62304, and 21 CFR Part 820. Reviews DHFs, technical files, and software validation and the operator should preserve the upstream workflow, copied support f...
Classify germline variants from VCF/BCF files according to the ACMG/AMP 2015 28-criteria evidence framework and
Pharmacogenomic report from DTC genetic data (23andMe/AncestryDNA) — 12 genes, 31 SNPs, 51 drugs
Medication photo to personalised PGx dosage card via Claude vision — snap a pill, get genotype-informed guidance
Assigns CDT codes with procedure-specific documentation and insurance submission requirements. Use when coding dental procedures, submitting dental claims, or managing CDT code selection.
IEC 62304 medical device software lifecycle framework. Risk classification, software safety classification (A/B/C), design control, verification, validation, and regulatory documentation for FDA/EU MDR submissions.
End-to-end DICOM workflow: parsing, anonymization/de-identification, conversion, structured reporting, PACS query/retrieve, and DICOMweb. Build automated medical imaging pipelines.
Medical code mapping and classification tools. ICD-10-CM/PCS, CPT, SNOMED CT, HCPCS, LOINC, RxNorm. Code validation, mapping between terminologies, HCC risk adjustment, and reimbursement modeling.
Generates structured personal injury demand summaries covering liability analysis, chronological injury documentation, itemized damages, and settlement positioning. Covers MVA, premises liability, product defect, and medical malpractice claims. Use when preparing settlement packages, demand lette...
Audit a rehabilitation or physical therapy platform end-to-end -- evaluate recovery metrics tracking (ROM, strength, balance, gait), patient-reported outcomes (DASH, LEFS, NDI, ODI, PROMIS), home exercise program personalization and compliance tracking, setback prediction with risk stratification...
Analyzes expert witness reports, depositions, and testimony to identify gaps in medical record review, map conflicts to the full record set, and produce impeachment and admissibility analysis with pinpoint citations. Use when reviewing expert reports for missing medical records, selective review ...
Drafts an IRB-ready Informed Consent Form (ICF) for FDA-regulated clinical trials compliant with 21 CFR 50.25, 50.27, and ICH-GCP. Use when drafting or revising consent documents for Phase I–IV trials, IND studies, or other FDA-regulated protocols requiring IRB submission.
Drafts regulatory-compliant informed consent forms for healthcare procedures, clinical trials, research participation, or professional services. Incorporates HIPAA, FDA, IRB/Common Rule, and ICH-GCP requirements as applicable. Use when drafting surgical consent, research participant agreements, c...
Produces a plain-language comparison of advance directives and POLST/MOLST forms, covering legal status, clinician signatures, emergency precedence, clinical appropriateness, and document coordination. Use when the user asks about advance directive vs. POLST, living will vs. DNR, which document E...
Creates verified, Bates-cited chronological summaries of medical records for litigation. Extracts treatment timelines, providers, diagnoses, procedures, medications, and causation evidence with every clinical fact traceable to a specific Bates range. Identifies gaps, inconsistencies, pre-existing...
Drafts Investigator Agreements for FDA-regulated clinical trials between sponsors and principal investigators. Covers 21 CFR Parts 50, 56, 312/812, ICH GCP E6(R2), IRB governance, data integrity, IP, indemnification, financial terms, and termination. Use when preparing clinical trial investigator...
Structures test validation with precision, accuracy, linearity, and reference range establishment. Use when validating new assays, documenting method comparisons, or establishing reference ranges.
Creates structured operative notes with findings, technique, specimens, and estimated blood loss. Use when dictating operative reports, documenting surgical procedures, or recording intraoperative findings.
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