MCP Radar
Serveur MCP

healthguard

io.tooloracle/healthguard
Santé Juridique et conformité Public et accessible MCP 2026-07-28

Ce que fait ce MCP

Supports healthcare compliance and safety workflows including medical-device and IVD classification, drug interactions, clinical trials, pharmacovigilance, HIPAA, and GDPR health-data checks.

Capacités

Outils

12 outils
adverse_event_report
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
Schéma d’entrée 
{'type': 'object', 'properties': {'severity': {'type': 'string', 'description': 'mild|moderate|severe|life_threatening|fatal'}, 'drug_name': {'type': 'string'}, 'reporter_type': {'type': 'string', 'description': 'healthcare_professional|patient|other'}, 'event_description': {'type': 'string'}}, 'additionalProperties': False}
clinical_trial_phases
Clinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
Schéma d’entrée 
{'type': 'object', 'properties': {'phase': {'type': 'string', 'description': 'PRECLINICAL, PHASE_I, PHASE_II, PHASE_III, PHASE_IV'}}, 'additionalProperties': False}
device_classification
MDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
Schéma d’entrée 
{'type': 'object', 'properties': {'active': {'type': 'boolean'}, 'duration': {'type': 'string', 'description': 'transient | short_term | long_term'}, 'invasive': {'type': 'boolean'}, 'surgical': {'type': 'boolean'}, 'measuring': {'type': 'boolean'}, 'implantable': {'type': 'boolean'}, 'body_orifice': {'type': 'boolean'}, 'nanomaterial': {'type': 'boolean'}, 'software_only': {'type': 'boolean'}}, 'additionalProperties': False}
drug_interaction
Basic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
Schéma d’entrée 
{'type': 'object', 'properties': {'drugs': {'type': 'string', 'description': 'Comma-separated drug names (min 2)'}}, 'additionalProperties': False}
gdpr_health_check
GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
Schéma d’entrée 
{'type': 'object', 'properties': {'purpose': {'type': 'string', 'description': 'Processing purpose'}, 'data_types': {'type': 'string', 'description': 'Comma-separated data types'}, 'cross_border_transfer': {'type': 'boolean'}}, 'additionalProperties': False}
gmp_checklist
Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
Schéma d’entrée 
{'type': 'object', 'properties': {'facility_type': {'type': 'string', 'description': 'manufacturing | packaging | testing | storage'}}, 'additionalProperties': False}
hipaa_vs_gdpr
HIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
Schéma d’entrée 
{'type': 'object', 'properties': {}, 'additionalProperties': False}
icd10_lookup
ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
Schéma d’entrée 
{'type': 'object', 'properties': {'code': {'type': 'string', 'description': 'ICD-10 code e.g. J06.9'}, 'search': {'type': 'string', 'description': 'Search term e.g. diabetes'}}, 'additionalProperties': False}
ivdr_check
EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
Schéma d’entrée 
{'type': 'object', 'properties': {'risk_class': {'type': 'string', 'description': 'A, B, C, or D'}, 'device_name': {'type': 'string'}}, 'additionalProperties': False}
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.
Schéma d’entrée 
{'type': 'object', 'properties': {'device_name': {'type': 'string', 'description': 'Device name'}, 'has_ce_mark': {'type': 'boolean'}, 'device_class': {'type': 'string', 'description': 'I, IIa, IIb, or III'}, 'udi_assigned': {'type': 'boolean'}, 'has_notified_body': {'type': 'boolean'}, 'eudamed_registered': {'type': 'boolean'}, 'clinical_evaluation': {'type': 'boolean'}, 'post_market_surveillance': {'type': 'boolean'}, 'quality_management_system': {'type': 'boolean'}}, 'additionalProperties': False}
medical_calendar_eu
EU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
Schéma d’entrée 
{'type': 'object', 'properties': {'year': {'type': 'integer', 'description': 'Year (default: 2026)'}}, 'additionalProperties': False}
udi_validate
Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
Schéma d’entrée 
{'type': 'object', 'properties': {'udi': {'type': 'string', 'description': 'UDI string to validate'}}, 'additionalProperties': False}
Historique

Modifications récentes des outils

Ajouté
medical_calendar_eu
17 September 2026 12:53
Ajouté
gmp_checklist
17 September 2026 12:53
Ajouté
clinical_trial_phases
17 September 2026 12:53
Ajouté
hipaa_vs_gdpr
17 September 2026 12:53
Ajouté
gdpr_health_check
17 September 2026 12:53
Ajouté
adverse_event_report
17 September 2026 12:53
Ajouté
icd10_lookup
17 September 2026 12:53
Ajouté
drug_interaction
17 September 2026 12:53
Ajouté
udi_validate
17 September 2026 12:53
Ajouté
device_classification
17 September 2026 12:53
Ajouté
ivdr_check
17 September 2026 12:53
Ajouté
mdr_compliance_check
17 September 2026 12:53
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