io.tooloracle/healthguard

repo:https://github.com/tooloracle/healthguard

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

transport:: remote
credential class:: self-provisionable
repo:: https://github.com/ToolOracle/healthguard

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Tools

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

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