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Found 816 Skills
When the user wants to optimize medical device distribution, manage device traceability, handle consignment inventory, or ensure regulatory compliance for medical devices. Also use when the user mentions "medical device logistics," "UDI compliance," "device traceability," "consignment management," "implant tracking," "loaner sets," "FDA compliance," "sterile device distribution," "recall management," or "GS1 standards." For hospital internal logistics, see hospital-logistics. For pharmaceutical distribution, see pharmacy-supply-chain.
Privacy-by-design analytics setup for clients operating under Uganda's Data Protection and Privacy Act 2019, Kenya's Data Protection Act 2019, and international frameworks (GDPR, CCPA). Covers cookie consent implementation, GA4 privacy configuration, data minimisation, and WhatsApp data governance. Invoke when setting up GA4 for a new client, configuring cookie consent banners, advising on analytics data governance, or when a client asks about data protection compliance for their digital channels. Does not replace legal counsel — flags compliance requirements and provides implementation guidance.
When the user wants to implement shipment tracking, product traceability, or supply chain visibility. Also use when the user mentions "tracking," "traceability," "visibility," "serialization," "lot tracking," "batch tracking," "chain of custody," "provenance," "track and trace," or "shipment monitoring." For control towers, see control-tower-design. For compliance, see compliance-management.
Derive security requirements from threat models and business context. Use when translating threats into actionable requirements, creating security user stories, or building security test cases.
Comprehensive toolkit for preparing ISO 13485 certification documentation for medical device Quality Management Systems. Use when users need help with ISO 13485 QMS documentation, including (1) conducting gap analysis of existing documentation, (2) creating Quality Manuals, (3) developing required procedures and work instructions, (4) preparing Medical Device Files, (5) understanding ISO 13485 requirements, or (6) identifying missing documentation for medical device certification. Also use when users mention medical device regulations, QMS certification, FDA QMSR, EU MDR, or need help with quality system documentation.
Initialize and manage the evidence collection directory for professional security audits with documented proof of findings.
Rapidly triage an incoming NDA and classify it as GREEN (standard approval), YELLOW (counsel review), or RED (full legal review). Use when a new NDA arrives from sales or business development, when screening for embedded non-solicits, non-competes, or missing carveouts, or when deciding whether an NDA can be signed under standard delegation.
安全自动化的专业技能和方法论
Assess and classify legal risks using a severity-by-likelihood framework with escalation criteria. Use when evaluating contract risk, assessing deal exposure, classifying issues by severity, or determining whether a matter needs senior counsel or outside legal review.
Map identified threats to appropriate security controls and mitigations. Use when prioritizing security investments, creating remediation plans, or validating control effectiveness.
Analyze Supabase authentication configuration for security weaknesses and misconfigurations.
Comprehensive Docker security guidelines and threat mitigation strategies