healthguard
Server Details
HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
- Status
- Healthy
- Uptime
- 100.0% over the last 24 hours
- Last Tested
- Transport
- Streamable HTTP · MCP 2025-03-26
- URL
- Repository
- ToolOracle/healthguard
- GitHub Stars
- 0
- ChatGPT
- –
- Claude
- –
TDQS
Scored across 12 tools
Most tools map to clearly distinct regulatory areas, such as device classification, GMP audits, or GDPR assessments. The closest pair is gdpr_health_check and hipaa_vs_gdpr, but one is an Art. 9 compliance assessment while the other is a cross-regime comparison, so they remain separable.
All names use snake_case and are broadly topic-prefixed, which aids readability. However, the set mixes noun-style names like device_classification and medical_calendar_eu with action-style names like udi_validate and icd10_lookup, and suffixes vary among check, checklist, compliance_check, lookup, and report.
Twelve tools is well within the ideal range and matches the broad healthcare regulatory compliance scope. Each tool covers a meaningful subdomain without the set feeling padded or overwhelming.
The toolkit covers medical devices, IVDs, pharmaceuticals, clinical trials, GMP, data protection, and ICD-10 coding, which is strong for its apparent purpose. Minor gaps exist, such as no actual AE submission workflow or dedicated vigilance/recall tooling, but agents can complete most common compliance checks without dead ends.
Available Tools
12 toolsadverse_event_reportAInspect
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
Inputs: severity, drug_name, reporter_type, event_description.
clinical_trial_phasesBInspect
Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
Inputs: phase.
device_classificationAInspect
MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
Inputs: active, duration, invasive, surgical, +5 more.
drug_interactionAInspect
Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
Inputs: drugs.
gdpr_health_checkAInspect
GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
Inputs: purpose, data_types, cross_border_transfer.
gmp_checklistBInspect
Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
Inputs: facility_type.
hipaa_vs_gdprAInspect
HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
Inputs: no named parameters.
icd10_lookupAInspect
ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
Inputs: code, search.
ivdr_checkDInspect
EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
Inputs: risk_class, device_name.
mdr_compliance_checkAInspect
EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
Inputs: device_name, has_ce_mark, device_class, udi_assigned, +5 more.
medical_calendar_euCInspect
EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
Inputs: year.
udi_validateAInspect
Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
Inputs: udi.
Tool Schema Changelog
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