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Healthguard

tooloracle/healthguard

This is a compliance-focused MCP for handling sensitive health data in AI workflows. It provides 12 tools centered on PII redaction and validation against HIPAA and GDPR Article 9 requirements for processing health information. Reach for this when you're building healthcare applications or chatbots that need to scrub patient data before it hits your LLM, or when you need programmatic checks that your prompts and responses meet medical data privacy standards. The streamable HTTP transport means you can deploy it as a service rather than running it locally. Useful if you're working with medical records, patient communications, or any health-related content where you need audit trails showing compliance measures were applied.

tools
12
transport
HTTP
last updated
May 7, 2026
View on GitHub

Install

From registry metadata
$ npx add-mcp https://tooloracle.io/health/mcp/ --name healthguard

Run in your terminal. add-mcp asks which agents to add it to (Claude Code, Codex, Cursor and more). Add -g to install it for every project.

Review the command, arguments and environment values before installing. MCP servers run with your local permissions.

Other ways

Claude Code

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

Run in your terminal. Add --scope user to make it available in every project.

Tools

Verified live · 12 tools

Verified live against the running server on Nov 6, 2026.

mdr_compliance_checkEU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.9 params

EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.

Parameters* required
clinical_evaluationboolean
device_classstring
I, IIa, IIb, or III
device_namestring
Device name
eudamed_registeredboolean
has_ce_markboolean
has_notified_bodyboolean
post_market_surveillanceboolean
quality_management_systemboolean
udi_assignedboolean
ivdr_checkEU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.2 params

EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.

Parameters* required
device_namestring
risk_classstring
A, B, C, or D
device_classificationMDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.9 params

MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.

Parameters* required
activeboolean
body_orificeboolean
durationstring
transient | short_term | long_term
implantableboolean
invasiveboolean
measuringboolean
nanomaterialboolean
software_onlyboolean
surgicalboolean
udi_validateValidate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).1 params

Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).

Parameters* required
udistring
UDI string to validate
drug_interactionBasic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.1 params

Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.

Parameters* required
drugsstring
Comma-separated drug names (min 2)
icd10_lookupICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).2 params

ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).

Parameters* required
codestring
ICD-10 code e.g. J06.9
searchstring
Search term e.g. diabetes
adverse_event_reportGenerate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.4 params

Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.

Parameters* required
drug_namestring
event_descriptionstring
reporter_typestring
healthcare_professional|patient|other
severitystring
mild|moderate|severe|life_threatening|fatal
gdpr_health_checkGDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.3 params

GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.

Parameters* required
cross_border_transferboolean
data_typesstring
Comma-separated data types
purposestring
Processing purpose
hipaa_vs_gdprHIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.

HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.

No parameters. Call it with no arguments.

clinical_trial_phasesClinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.1 params

Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.

Parameters* required
phasestring
PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV
gmp_checklistGood Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.1 params

Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.

Parameters* required
facility_typestring
manufacturing | packaging | testing | storage
medical_calendar_euEU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.1 params

EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.

Parameters* required
yearinteger
Year (default: 2026)

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Readme

HealthGuard MCP Server v1.0.0

Healthcare Compliance MCP Server — 12 tools for EU MDR/IVDR medical device regulation, pharmacovigilance, ICD-10 coding, GMP audits, GDPR health data (Art.9), clinical trial phases (EU CTR), HIPAA vs GDPR comparison.

Port 12401 | Part of ToolOracle & FeedOracle Infrastructure

Quick Connect

# Claude Desktop / Claude Code
claude mcp add healthguard https://tooloracle.io/health-guard/mcp

# Or use directly
curl -X POST https://tooloracle.io/health-guard/mcp/ \
  -H "Content-Type: application/json" \
  -d '{"jsonrpc":"2.0","id":1,"method":"tools/list"}'

12 Tools

| mdr_compliance_check | Tool 1 | | ivdr_check | Tool 2 | | device_classification | Tool 3 | | udi_validate | Tool 4 | | drug_interaction | Tool 5 | | icd10_lookup | Tool 6 | | adverse_event_report | Tool 7 | | gdpr_health_check | Tool 8 | | hipaa_vs_gdpr | Tool 9 | | clinical_trial_phases | Tool 10 | | gmp_checklist | Tool 11 | | medical_calendar_eu | Tool 12 |

Endpoints

View the full README on GitHub

Details

Repository
github.com/tooloracle/healthguard
Transport
HTTP
Registry
MCP registry, active
Tools verified
Nov 6, 2026

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