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io.tooloracle/healthguard

io.tooloracle/healthguard · v1.0.0

No registry update 90+ days

Measured by MCP Station

Last check	Reachable
Checked at	—
Check success 7 / 30 days	—
First-try success 30 days	—
Median response	—
Lookups 30 days	—
Authentication	No auth
MCP version	2025-03-26
Rank score	—
Declared risk	Not declared (tools carry no read/destructive hints)
Capabilities declared	tools
Tool definitions	12 tools · with description 100% · input schema is an object 100% · read/destructive hints 0%

Description written by the publisher, not verified

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

Connect

streamable-http · https://tooloracle.io/health/mcp/

claude mcp add --transport http healthguard https://tooloracle.io/health/mcp/

{
  "mcpServers": {
    "healthguard": {
      "url": "https://tooloracle.io/health/mcp/"
    }
  }
}

Tools as reported by the server

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

Repository · JSON · Text for agents · Registry updated 2026-05-07