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Found 39 Skills
This skill should be used when the user asks to "generate audit logs", "create HIPAA audit trail", "log healthcare events", "configure audit logging", "track PHI access", "maintain compliance logs", "audit log format", "healthcare event logging", "access control logging", "authentication logging", "HIPAA logging requirements", or mentions HIPAA audit trails, healthcare event logging, compliance logging, PHI access tracking, authentication auditing, or §164.312(b) logging requirements.
Generate concise (3-4 page), focused medical treatment plans in LaTeX/PDF format for all clinical specialties. Supports general medical treatment, rehabilitation therapy, mental health care, chronic disease management, perioperative care, and pain management. Includes SMART goal frameworks, evidence-based interventions with minimal text citations, regulatory compliance (HIPAA), and professional formatting. Prioritizes brevity and clinical actionability.
FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and device cybersecurity. Use when user mentions FDA submission, 510(k), PMA, De Novo, QSR, premarket, predicate device, substantial equivalence, HIPAA medical device, or FDA cybersecurity.
Regulatory compliance testing for GDPR, CCPA, HIPAA, SOC2, PCI-DSS and industry-specific regulations. Use when ensuring legal compliance, preparing for audits, or handling sensitive data.
Plan healthcare privacy, research, and regulatory compliance for a digital health product, including HIPAA, IRB, FDA, GDPR, governance, and operational controls.
Senior FDA consultant and specialist for medical device companies including HIPAA compliance and requirement management. Provides FDA pathway expertise, QSR compliance, cybersecurity guidance, and regulatory submission support. Use for FDA submission planning, QSR compliance assessments, HIPAA evaluations, and FDA regulatory strategy development.
Generate legally-sound terms of service, privacy policies, and medical disclaimers for recovery and wellness applications. Expert in HIPAA, GDPR, CCPA compliance. Activate on 'terms of service', 'privacy policy', 'legal terms', 'medical disclaimer', 'HIPAA', 'user agreement'. NOT for contract negotiation (use attorney), app development (use domain skills), or moderation (use recovery-community-moderator).
You are a compliance expert specializing in regulatory requirements for software systems including GDPR, HIPAA, SOC2, PCI-DSS, and other industry standards. Perform compliance audits and provide implementation guidance.
Draft and fill data privacy agreement templates — DPA, data processing agreement, GDPR, HIPAA BAA, business associate agreement, AI addendum. Produces signable DOCX files from Common Paper standard forms.
Use this skill when preparing for SOC 2, HIPAA, or PCI-DSS compliance, conducting audits, or implementing security controls. Triggers on SOC 2, HIPAA, PCI-DSS, compliance audit, security controls, risk assessment, control frameworks, and any task requiring regulatory compliance planning or audit preparation.
Use when handling authentication, authorization, encryption, HIPAA compliance, SOC 2, privacy policies, penetration testing, or any security and compliance concerns
Audit and consolidate documentation for healthcare engineering systems. Supports two modes — analyze (coverage audit — writes only .health-docs/analysis.md) and document (consolidate existing docs + fill gaps). Detects applicable regulatory regimes (HIPAA, ONC, FDA SaMD) from codebase signals, composes existing skills as subagents for deep-dimension analysis, and produces a structured handoff artifact consumed by document mode.