healthguard
HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
使うべきか
品質と安全性
検出事項（4）
- LOWTool 'ivdr_check' description lacks action verbivdr_check 内
- LOWTool 'hipaa_vs_gdpr' description lacks action verbhipaa_vs_gdpr 内
- LOWTool 'clinical_trial_phases' description lacks action verbclinical_trial_phases 内
- LOWTool 'medical_calendar_eu' description lacks action verbmedical_calendar_eu 内
ツール定義とプロトコルへの準拠に関する自動分析に基づいています。
コンテキストコスト
これは、サーバーのツールがモデルのコンテキストに読み込まれるたびに消費されるおおよそのトークン数です。数が多いほど、ほかのタスクに使える注意が減ります。
インストール
ワンクリックインストール
これを `claude_desktop_config.json` ファイルに追加してください:
{
"mcpServers": {
"healthguard": {
"url": "https://tooloracle.io/health/mcp/"
}
}
}リモートエンドポイント
https://tooloracle.io/health/mcp/streamable-httpできること
ツール一覧
ツール（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.
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"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).
入力スキーマ
{
"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.
入力スキーマ
{
"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).
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"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.
入力スキーマ
{
"type": "object",
"properties": {
"year": {
"type": "integer",
"description": "Year (default: 2026)"
}
},
"additionalProperties": false
}コミュニティ
エビデンス