healthguard
Server Details
HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
- Status
- Healthy
- Last Tested
- Transport
- Streamable HTTP
- URL
- Repository
- ToolOracle/healthguard
- GitHub Stars
- 0
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Tool Definition Quality
Average 3.5/5 across 12 of 12 tools scored. Lowest: 2.7/5.
Each tool addresses a distinct aspect of healthcare regulatory compliance (e.g., adverse events, clinical trials, device classification, GDPR, GMP, ICD-10, IVDR, MDR, UDI). No two tools have overlapping purposes, ensuring clear differentiation.
All tool names use a consistent snake_case pattern with descriptive noun_phrase or acronym_action structure (e.g., adverse_event_report, icd10_lookup, mdr_compliance_check). No mixing of conventions.
The 12 tools cover a comprehensive range of healthcare regulatory topics without being excessive. Each tool serves a clear purpose, and the count is well-scoped for the server's stated domain.
The tool set covers major EU healthcare regulatory areas (MDR, IVDR, GMP, GDPR, clinical trials, drug interactions, UDI). Minor gaps exist, such as lack of a dedicated EUDAMED registration tool or a more comprehensive quality management system tool, but overall coverage is substantial.
Available Tools
12 toolsadverse_event_reportInspect
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
| Name | Required | Description | Default |
|---|---|---|---|
| severity | No | mild|moderate|severe|life_threatening|fatal | |
| drug_name | No | ||
| reporter_type | No | healthcare_professional|patient|other | |
| event_description | No |
clinical_trial_phasesInspect
Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
| Name | Required | Description | Default |
|---|---|---|---|
| phase | No | PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV |
device_classificationInspect
MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
| Name | Required | Description | Default |
|---|---|---|---|
| active | No | ||
| duration | No | transient | short_term | long_term | |
| invasive | No | ||
| surgical | No | ||
| measuring | No | ||
| implantable | No | ||
| body_orifice | No | ||
| nanomaterial | No | ||
| software_only | No |
drug_interactionInspect
Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
| Name | Required | Description | Default |
|---|---|---|---|
| drugs | No | Comma-separated drug names (min 2) |
gdpr_health_checkInspect
GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
| Name | Required | Description | Default |
|---|---|---|---|
| purpose | No | Processing purpose | |
| data_types | No | Comma-separated data types | |
| cross_border_transfer | No |
gmp_checklistInspect
Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
| Name | Required | Description | Default |
|---|---|---|---|
| facility_type | No | manufacturing | packaging | testing | storage |
hipaa_vs_gdprInspect
HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
| Name | Required | Description | Default |
|---|---|---|---|
No parameters | |||
icd10_lookupInspect
ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
| Name | Required | Description | Default |
|---|---|---|---|
| code | No | ICD-10 code e.g. J06.9 | |
| search | No | Search term e.g. diabetes |
ivdr_checkInspect
EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
| Name | Required | Description | Default |
|---|---|---|---|
| risk_class | No | A, B, C, or D | |
| device_name | No |
mdr_compliance_checkInspect
EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
| Name | Required | Description | Default |
|---|---|---|---|
| device_name | No | Device name | |
| has_ce_mark | No | ||
| device_class | No | I, IIa, IIb, or III | |
| udi_assigned | No | ||
| has_notified_body | No | ||
| eudamed_registered | No | ||
| clinical_evaluation | No | ||
| post_market_surveillance | No | ||
| quality_management_system | No |
medical_calendar_euInspect
EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
| Name | Required | Description | Default |
|---|---|---|---|
| year | No | Year (default: 2026) |
udi_validateInspect
Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
| Name | Required | Description | Default |
|---|---|---|---|
| udi | No | UDI string to validate |
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