HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
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Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
mild|moderate|severe|life_threatening|fatal
healthcare_professional|patient|other
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Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
| Argument | Type | Description |
|---|---|---|
| severity | string | mild|moderate|severe|life_threatening|fatal |
| drug_name | string | |
| reporter_type | string | healthcare_professional|patient|other |
| event_description | string |
{
"type": "object",
"properties": {
"severity": {
"type": "string",
"description": "mild|moderate|severe|life_threatening|fatal"
},
"drug_name": {
"type": "string"
},
"reporter_type": {
"type": "string",
"description": "healthcare_professional|patient|other"
},
"event_description": {
"type": "string"
}
},
"additionalProperties": false
}Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
| Argument | Type | Description |
|---|---|---|
| phase | string | PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV |
{
"type": "object",
"properties": {
"phase": {
"type": "string",
"description": "PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV"
}
},
"additionalProperties": false
}MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
| Argument | Type | Description |
|---|---|---|
| active | boolean | |
| duration | string | transient | short_term | long_term |
| invasive | boolean | |
| surgical | boolean | |
| measuring | boolean | |
| implantable | boolean | |
| body_orifice | boolean | |
| nanomaterial | boolean | |
| software_only | boolean |
{
"type": "object",
"properties": {
"active": {
"type": "boolean"
},
"duration": {
"type": "string",
"description": "transient | short_term | long_term"
},
"invasive": {
"type": "boolean"
},
"surgical": {
"type": "boolean"
},
"measuring": {
"type": "boolean"
},
"implantable": {
"type": "boolean"
},
"body_orifice": {
"type": "boolean"
},
"nanomaterial": {
"type": "boolean"
},
"software_only": {
"type": "boolean"
}
},
"additionalProperties": false
}Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
| Argument | Type | Description |
|---|---|---|
| drugs | string | Comma-separated drug names (min 2) |
{
"type": "object",
"properties": {
"drugs": {
"type": "string",
"description": "Comma-separated drug names (min 2)"
}
},
"additionalProperties": false
}GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
| Argument | Type | Description |
|---|---|---|
| purpose | string | Processing purpose |
| data_types | string | Comma-separated data types |
| cross_border_transfer | boolean |
{
"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
}Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
| Argument | Type | Description |
|---|---|---|
| facility_type | string | manufacturing | packaging | testing | storage |
{
"type": "object",
"properties": {
"facility_type": {
"type": "string",
"description": "manufacturing | packaging | testing | storage"
}
},
"additionalProperties": false
}HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
No arguments.
{
"type": "object",
"properties": {},
"additionalProperties": false
}ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
| Argument | Type | Description |
|---|---|---|
| code | string | ICD-10 code e.g. J06.9 |
| search | string | Search term e.g. diabetes |
{
"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
}EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
| Argument | Type | Description |
|---|---|---|
| risk_class | string | A, B, C, or D |
| device_name | string |
{
"type": "object",
"properties": {
"risk_class": {
"type": "string",
"description": "A, B, C, or D"
},
"device_name": {
"type": "string"
}
},
"additionalProperties": false
}EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
| Argument | Type | Description |
|---|---|---|
| device_name | string | Device name |
| has_ce_mark | boolean | |
| device_class | string | I, IIa, IIb, or III |
| udi_assigned | boolean | |
| has_notified_body | boolean | |
| eudamed_registered | boolean | |
| clinical_evaluation | boolean | |
| post_market_surveillance | boolean | |
| quality_management_system | boolean |
{
"type": "object",
"properties": {
"device_name": {
"type": "string",
"description": "Device name"
},
"has_ce_mark": {
"type": "boolean"
},
"device_class": {
"type": "string",
"description": "I, IIa, IIb, or III"
},
"udi_assigned": {
"type": "boolean"
},
"has_notified_body": {
"type": "boolean"
},
"eudamed_registered": {
"type": "boolean"
},
"clinical_evaluation": {
"type": "boolean"
},
"post_market_surveillance": {
"type": "boolean"
},
"quality_management_system": {
"type": "boolean"
}
},
"additionalProperties": false
}EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
| Argument | Type | Description |
|---|---|---|
| year | integer | Year (default: 2026) |
{
"type": "object",
"properties": {
"year": {
"type": "integer",
"description": "Year (default: 2026)"
}
},
"additionalProperties": false
}Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
| Argument | Type | Description |
|---|---|---|
| udi | string | UDI string to validate |
{
"type": "object",
"properties": {
"udi": {
"type": "string",
"description": "UDI string to validate"
}
},
"additionalProperties": false
}