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Healthguard

by tooloracle.io in Other

MCP serverPassing, checked 2 h ago

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

https://tooloracle.io/health/mcp/

Last 30 days

All checks passedSome failedAll failedNot checked
Uptime
100%
Response time
115 ms typical, 115 ms slowest 5%
Last check
2 h ago
Next check
in 5 h

How to call it

Add it to any MCP client that supports remote servers.

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

12 tools

  • 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.

Security scan

  • No findings. We scan names, descriptions and tool definitions for hidden instructions and other prompt-injection patterns.

Recent checks

WhenResultHTTPTime
2 h agoPassed200111 ms
12 h agoPassed200115 ms
22 h agoPassed200175 ms