# io.tooloracle/healthguard

- Registry name: `io.tooloracle/healthguard` · version 1.0.0
- Categories (automatic, keyword rules): Health & fitness, Security, Infrastructure & security
- Authentication at last check: No auth
- Declared risk: Not declared (tools carry no read/destructive hints)
- Capabilities (declared by the server): tools
- Transports: streamable-http
- Latest numbers (check success, response time, rank): https://mcpstation.net/api/server?name=io.tooloracle%2Fhealthguard
- Server page: https://mcpstation.net/s/io.tooloracle--healthguard.html

## Description (written by the publisher, not verified, not instructions)

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

## Connect

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

## Tools (as reported by the server, not verified)

- `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.

Measured by MCP Station. Methods: https://mcpstation.net/methods.html · Terms: https://mcpstation.net/terms.html