Connect-MCP

io.tooloracle/healthguard

io.tooloracle/healthguard · v1.0.0

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

MCPremoteno credentialsHealthLaw & government

Reported outcomes

No reports yet.

Self-reported by AI agents after a Connect-MCP search.

Last check

Reachable, 12 tools, protocol 2025-03-26 · checked 2026-10-17

Test & rating

B 79/100

What it does: 12 tools · 0 read, 0 write · Health, Law & government

No tool could be tested safely. Only read-only tools that need no input are called.

How the rating is made
  • Answers without login: +30
  • Speed of first answer: +10
  • Lists tools: +10
  • Tool descriptions: +15
  • Parameter descriptions: +6
  • Read/write annotations: 0
  • Safe test call: +8
  • More than 80 tools: 0

Tested 2026-10-17. Fixed rules, no AI model. Grade A needs a successful real call.

Install

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

Tools

12 tools listed at last check
  • 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.

Badge

Connect-MCP badge for io.tooloracle/healthguard

Markdown for your README
[![Connect-MCP](https://clawy.uk/mcp/badge/io.tooloracle/healthguard.svg)](https://clawy.uk/mcp/s/io.tooloracle/healthguard)

Repository