healthguard
HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
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Calidad y seguridad
Hallazgos (4)
- LOWTool 'ivdr_check' description lacks action verben ivdr_check
- LOWTool 'hipaa_vs_gdpr' description lacks action verben hipaa_vs_gdpr
- LOWTool 'clinical_trial_phases' description lacks action verben clinical_trial_phases
- LOWTool 'medical_calendar_eu' description lacks action verben medical_calendar_eu
Basado en el análisis automatizado de las definiciones de herramientas y el cumplimiento del protocolo.
Costo de contexto
Este es el número aproximado de tokens que se consumen cada vez que las herramientas del servidor se cargan en el contexto de un modelo. Los recuentos más altos reducen la atención disponible para otras tareas.
Instalar
Instalación con un clic
Agrega esto a tu archivo `claude_desktop_config.json`:
{
"mcpServers": {
"healthguard": {
"url": "https://tooloracle.io/health/mcp/"
}
}
}Puntos de conexión remotos
https://tooloracle.io/health/mcp/streamable-httpQué puede hacer
Inventario de herramientas
Herramientas (12)
🟢mdr_compliance_check(device_name, device_class, has_ce_mark, has_notified_body, clinical_evaluation, ...)
EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
Esquema de entrada
{
"type": "object",
"properties": {
"device_name": {
"type": "string",
"description": "Device name"
},
"device_class": {
"type": "string",
"description": "I, IIa, IIb, or III"
},
"has_ce_mark": {
"type": "boolean"
},
"has_notified_body": {
"type": "boolean"
},
"clinical_evaluation": {
"type": "boolean"
},
"post_market_surveillance": {
"type": "boolean"
},
"udi_assigned": {
"type": "boolean"
},
"quality_management_system": {
"type": "boolean"
},
"eudamed_registered": {
"type": "boolean"
}
},
"additionalProperties": false
}🟢ivdr_check(device_name, risk_class)
EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
Esquema de entrada
{
"type": "object",
"properties": {
"device_name": {
"type": "string"
},
"risk_class": {
"type": "string",
"description": "A, B, C, or D"
}
},
"additionalProperties": false
}⚪device_classification(invasive, implantable, active, duration, body_orifice, ...)
MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
Esquema de entrada
{
"type": "object",
"properties": {
"invasive": {
"type": "boolean"
},
"implantable": {
"type": "boolean"
},
"active": {
"type": "boolean"
},
"duration": {
"type": "string",
"description": "transient | short_term | long_term"
},
"body_orifice": {
"type": "boolean"
},
"surgical": {
"type": "boolean"
},
"software_only": {
"type": "boolean"
},
"nanomaterial": {
"type": "boolean"
},
"measuring": {
"type": "boolean"
}
},
"additionalProperties": false
}⚪udi_validate(udi)
Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
Esquema de entrada
{
"type": "object",
"properties": {
"udi": {
"type": "string",
"description": "UDI string to validate"
}
},
"additionalProperties": false
}⚪drug_interaction(drugs)
Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
Esquema de entrada
{
"type": "object",
"properties": {
"drugs": {
"type": "string",
"description": "Comma-separated drug names (min 2)"
}
},
"additionalProperties": false
}⚪icd10_lookup(code, search)
ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
Esquema de entrada
{
"type": "object",
"properties": {
"code": {
"type": "string",
"description": "ICD-10 code e.g. J06.9"
},
"search": {
"type": "string",
"description": "Search term e.g. diabetes"
}
},
"additionalProperties": false
}⚪adverse_event_report(drug_name, event_description, severity, reporter_type)
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
Esquema de entrada
{
"type": "object",
"properties": {
"drug_name": {
"type": "string"
},
"event_description": {
"type": "string"
},
"severity": {
"type": "string",
"description": "mild|moderate|severe|life_threatening|fatal"
},
"reporter_type": {
"type": "string",
"description": "healthcare_professional|patient|other"
}
},
"additionalProperties": false
}🟢gdpr_health_check(purpose, data_types, cross_border_transfer)
GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
Esquema de entrada
{
"type": "object",
"properties": {
"purpose": {
"type": "string",
"description": "Processing purpose"
},
"data_types": {
"type": "string",
"description": "Comma-separated data types"
},
"cross_border_transfer": {
"type": "boolean"
}
},
"additionalProperties": false
}⚪hipaa_vs_gdpr
HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
Esquema de entrada
{
"type": "object",
"properties": {},
"additionalProperties": false
}⚪clinical_trial_phases(phase)
Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
Esquema de entrada
{
"type": "object",
"properties": {
"phase": {
"type": "string",
"description": "PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV"
}
},
"additionalProperties": false
}⚪gmp_checklist(facility_type)
Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
Esquema de entrada
{
"type": "object",
"properties": {
"facility_type": {
"type": "string",
"description": "manufacturing | packaging | testing | storage"
}
},
"additionalProperties": false
}⚪medical_calendar_eu(year)
EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
Esquema de entrada
{
"type": "object",
"properties": {
"year": {
"type": "integer",
"description": "Year (default: 2026)"
}
},
"additionalProperties": false
}Comunidad
Evidencia