{"serverId":"mcp-registry/io.tooloracle/healthguard","tools":[{"name":"gdpr_health_check","fixed":{"name":"gdpr_health_check","description":"GDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.","inputSchema":{"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},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":119,"tokensAfter":119},{"name":"gmp_checklist","fixed":{"name":"gmp_checklist","description":"Good Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.","inputSchema":{"type":"object","properties":{"facility_type":{"type":"string","description":"manufacturing | packaging | testing | storage"}},"additionalProperties":false},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":95,"tokensAfter":95},{"name":"icd10_lookup","fixed":{"name":"icd10_lookup","description":"ICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).","inputSchema":{"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},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":100,"tokensAfter":100},{"name":"ivdr_check","fixed":{"name":"ivdr_check","description":"EU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.","inputSchema":{"type":"object","properties":{"risk_class":{"type":"string","description":"A, B, C, or D"},"device_name":{"type":"string"}},"additionalProperties":false},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":92,"tokensAfter":92},{"name":"mdr_compliance_check","fixed":{"name":"mdr_compliance_check","description":"EU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.","inputSchema":{"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},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":194,"tokensAfter":194},{"name":"udi_validate","fixed":{"name":"udi_validate","description":"Validate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).","inputSchema":{"type":"object","properties":{"udi":{"type":"string","description":"UDI string to validate"}},"additionalProperties":false},"annotations":{"readOnlyHint":true}},"changes":[{"kind":"annotations","detail":"Added readOnlyHint: true (inferred from the name).","verify":true}],"tokensBefore":82,"tokensAfter":82}],"toolsChanged":6,"tokensSaved":0,"todo":[{"tool":"adverse_event_report","params":["drug_name","event_description"]},{"tool":"device_classification","params":["active","invasive","surgical","measuring","implantable","body_orifice","nanomaterial","software_only"]},{"tool":"gdpr_health_check","params":["cross_border_transfer"]},{"tool":"ivdr_check","params":["device_name"]},{"tool":"mdr_compliance_check","params":["has_ce_mark","udi_assigned","has_notified_body","eudamed_registered","clinical_evaluation","post_market_surveillance","quality_management_system"]}],"note":"Deterministic fixes. Changes marked verify need a human look before shipping (renames, inferred annotations, inferred types, removed text). Parameter descriptions in `todo` need to be written by someone who knows the API."}