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registry/healthguard
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healthguard

HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.

Tools 12
GitHub stars
Installs / wk
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Transport streamable-http
Last checked 26h ago

Tools & capabilities

12 tools

Read from the running server on 26h ago.

adverse_event_report severitydrug_namereporter_typeevent_description
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
clinical_trial_phases phase
Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
device_classification activedurationinvasivesurgicalmeasuringimplantable +3
MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
drug_interaction drugs
Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
gdpr_health_check purposedata_typescross_border_transfer
GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
gmp_checklist facility_type
Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
hipaa_vs_gdpr
HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
icd10_lookup codesearch
ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
ivdr_check risk_classdevice_name
EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
mdr_compliance_check device_namehas_ce_markdevice_classudi_assignedhas_notified_bodyeudamed_registered +3
EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
medical_calendar_eu year
EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
udi_validate udi
Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).