「hipaa」の検索結果

Guides DPIA for health and medical data processing covering Art. 9(2)(h)-(j) exemptions, HIPAA crosswalk for transatlantic operations, clinical trial data protection under EU CTR 536/2014, and genetic data specifics under Art. 9(1). Activate for healthcare systems, clinical research, health apps, or medical device data. Keywords: health data, DPIA, Art. 9, clinical trial, genetic data, HIPAA, medical records, special category.

日本語の概要は準備中です。原文の説明を表示しています。

Addresses HIPAA privacy and security requirements for health data interoperability under the 21st Century Cures Act, ONC Health IT Certification Program, and CMS Interoperability and Patient Access Final Rule. Covers information blocking prohibitions, FHIR API patient access, TEFCA exchange purposes, and privacy safeguards for health information exchange. Keywords: interoperability, information blocking, FHIR, TEFCA, Cures Act, patient access API, health information exchange.

日本語の概要は準備中です。原文の説明を表示しています。

Harmonises data classification across jurisdictions mapping GDPR special categories vs CCPA sensitive PI (1798.140(ae)) vs HIPAA PHI (160.103) vs LGPD sensitive data (Art. 5-II). Provides cross-regulation mapping matrix for multinational compliance. Keywords: cross-jurisdiction, GDPR, CCPA, HIPAA, LGPD, sensitive data, multinational, classification mapping.

日本語の概要は準備中です。原文の説明を表示しています。

Ensure HIPAA compliance when handling PHI (Protected Health Information). Use when writing code that accesses user health data, check-ins, journal entries, or any sensitive information. Activates for audit logging, data access, security events, and compliance questions.

日本語の概要は準備中です。原文の説明を表示しています。

FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QMSR (21 CFR 820, which incorporates ISO 13485:2016 by reference since 2026-02-02; formerly QSR) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QMSR, QSR, ISO 13485 for FDA, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.

日本語の概要は準備中です。原文の説明を表示しています。

Clinical-grade PII/PHI detection and de-identification for healthcare text data. Scans all 18 HIPAA identifier categories with confidence scoring, generates audit logs, supports custom regex patterns, and produces de-identified output while preserving document structure.

日本語の概要は準備中です。原文の説明を表示しています。

Implement HIPAA security and privacy rules. Configure PHI protections and BAA requirements. Use when handling healthcare data.

日本語の概要は準備中です。原文の説明を表示しています。

FDA regulatory consultant for medical device companies, covering 510(k)/PMA/De Novo pathways, QSR (21 CFR 820), HIPAA, and device cybersecurity. Use for FDA submissions, predicate and substantial-equivalence analysis, and premarket strategy.

日本語の概要は準備中です。原文の説明を表示しています。

HIPAA compliance - PHI protection, technical/administrative/physical safeguards, minimum necessary standard, BAA requirements, de-identification, access logging

日本語の概要は準備中です。原文の説明を表示しています。

Enterprise-grade compliance architecture for SOC 2, HIPAA, GDPR, PCI-DSS. Provides compliance checklists, security controls, audit guidance, and regulatory requirements for serverless and cloud architectures. Activates for compliance, HIPAA, SOC2, SOC 2, GDPR, PCI-DSS, PCI DSS, regulatory, healthcare data, payment card, data protection, audit, security standards, regulated industry, BAA, business associate agreement, DPIA, data protection impact assessment.

日本語の概要は準備中です。原文の説明を表示しています。

US state privacy law applicability assessment tool. Evaluates revenue thresholds, data volume thresholds, business exemptions (GLBA, HIPAA, nonprofits), employee data carve-outs, and SBA small business determinations across all enacted state privacy laws.

日本語の概要は準備中です。原文の説明を表示しています。

Implements 42 CFR Part 2 protections for substance use disorder patient records. Covers written consent requirements stricter than HIPAA, re-disclosure prohibition, court order procedures, qualified service organization agreements, and 2024 amendments aligning Part 2 with HIPAA. Keywords: 42 CFR Part 2, substance use disorder, SUD records, re-disclosure, consent, Part 2 amendments.

日本語の概要は準備中です。原文の説明を表示しています。

Implement tamper-evident audit logs for compliance (SOC 2, HIPAA, PCI DSS). Use when building compliance audit trails, tracking who did what and when, or implementing immutable event logs that satisfy regulatory retention requirements.

日本語の概要は準備中です。原文の説明を表示しています。

AWS Compliance Checker workflow skill. Use this skill when the user needs Automated compliance checking against CIS, PCI-DSS, HIPAA, and SOC 2 benchmarks and the operator should preserve the upstream workflow, copied support files, and provenance before merging or handing off.

日本語の概要は準備中です。原文の説明を表示しています。

AWS Compliance Checker workflow skill. Use this skill when the user needs Automated compliance checking against CIS, PCI-DSS, HIPAA, and SOC 2 benchmarks and the operator should preserve the upstream workflow, copied support files, and provenance before merging or handing off.

日本語の概要は準備中です。原文の説明を表示しています。

Automatically detect and de-identify PII (Personal Identifiable Information) and PHI (Protected Health Information) from clinical/medical text to ensure HIPAA compliance. Trigger when processing medical records, patient data, clinical notes, insurance information, or any healthcare-related text containing potential patient identifiers.

日本語の概要は準備中です。原文の説明を表示しています。

Use when writing clinical notes, documenting sessions, creating treatment plans for insurance/authorization, ensuring HIPAA compliance, or need structured documentation templates. Provides SOAP notes, progress notes (DAP format), and treatment plan templates. HIPAA-compliant guidance included.

日本語の概要は準備中です。原文の説明を表示しています。

Validates and summarizes the four required authorization forms in a personal injury matter (retainer, HIPAA release, insurance authorization, employment record release). Confirms signatures, dates, scope, and completeness to determine readiness for the investigation phase. Use when reviewing client onboarding packets, verifying authorization forms before discovery, or checking HIPAA and record-release compliance.

日本語の概要は準備中です。原文の説明を表示しています。

Use this skill when configuring Health Cloud patient consent management: setting up HIPAA authorization forms, consent templates, consent tracking per patient, and withdrawal handling. NOT for querying the AuthorizationFormConsent object hierarchy or its required field values — use data/consent-data-model-health. NOT for GDPR/CCPA marketing opt-out on ContactPointTypeConsent — use security/gdpr-data-privacy.

日本語の概要は準備中です。原文の説明を表示しています。

Validates and summarizes the four required authorization forms in a personal injury matter (retainer, HIPAA release, insurance authorization, employment record release). Confirms signatures, dates, scope, and completeness to determine readiness for the investigation phase. Use when reviewing client onboarding packets, verifying authorization forms before discovery, or checking HIPAA and record-release compliance.

日本語の概要は準備中です。原文の説明を表示しています。

Drafts jurisdiction-specific Advance Health Care Directive packages with agent appointment, living will instructions, HIPAA authorization bridge, organ donation preferences, and execution compliance checklists. Trigger when the user mentions advance directive, healthcare proxy, living will, health care agent, HIPAA authorization, medical power of attorney, end-of-life planning, capacity trigger planning, state-specific directive forms, witness/notary requirements for healthcare documents, or cross-state directive portability.

日本語の概要は準備中です。原文の説明を表示しています。

Automated compliance checking against CIS, PCI-DSS, HIPAA, and SOC 2 benchmarks

日本語の概要は準備中です。原文の説明を表示しています。

Automated compliance checking against CIS, PCI-DSS, HIPAA, and SOC 2 benchmarks

日本語の概要は準備中です。原文の説明を表示しています。

Expert en conformité (SOC2, ISO27001, GDPR, PCI-DSS, HIPAA, audits)

日本語の概要は準備中です。原文の説明を表示しています。