Total 30,035 skills, Security & Compliance has 1057 skills
Showing 12 of 1057 skills
List and review Google Workspace security alerts from Alert Center.
Use this skill when the user asks to scan a transaction, check transaction safety, is this transaction safe, pre-execution check, security scan, tx risk check, check if this approve is safe, scan this swap tx, is this token safe, check token security, honeypot check, is this URL a scam, check if this dapp is safe, phishing site check, is this signature safe, check this signing request, check my approvals, show risky approvals, revoke approval, token authorization, ERC20 allowance, Permit2, or mentions transaction security scanning, token risk scanning, DApp/URL phishing detection, message signature safety, pre-execution risk analysis, malicious transaction detection, approval safety checks, or token approval management. Covers token-scan (batch token risk detection), dapp-scan (URL/domain phishing detection), tx-scan (EVM + Solana transaction pre-execution), sig-scan (EIP-712/personal_sign message scanning), and approvals (ERC-20 allowance and Permit2 authorization queries). Chinese: 安全扫描, 代币安全, 蜜罐检测, 貔貅盘, 钓鱼网站, 交易安全, 签名安全, 代币风险, 授权管理, 授权查询, 风险授权, 代币授权. Do NOT use for wallet balance, send, or history — use okx-agentic-wallet. Do NOT use for general programming questions about security.
Use this skill when the user asks to export audit logs, find audit log location, view command history, 导出日志, 查看日志, 日志路径, 操作记录, 调用记录, 命令历史. Do NOT use for wallet balance, token search, swap, or any other on-chain operation — use the corresponding skill instead.
This skill provides guidance and enforcement rules for implementing secure two-factor authentication (2FA) using Better Auth's twoFactor plugin.
Generate Privy wallet policy rules from natural language. Use when the user wants to set up, modify, or review wallet security policies — transfer limits, address allowlists, method restrictions, time windows, etc.
Master smart contract security best practices to prevent common vulnerabilities and implement secure Solidity patterns. Use when writing smart contracts, auditing existing contracts, or implementing security measures for blockchain applications.
Implement GDPR-compliant data handling with consent management, data subject rights, and privacy by design. Use when building systems that process EU personal data, implementing privacy controls, or conducting GDPR compliance reviews.
Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides overall quality system responsibility, regulatory compliance oversight, management accountability, and strategic quality leadership. Use for quality system governance, regulatory compliance oversight, management responsibility, and quality strategic planning.
EU MDR 2017/745 regulation specialist and consultant for medical device requirement management. Provides comprehensive MDR compliance expertise, gap analysis, technical documentation guidance, clinical evidence requirements, and post-market surveillance implementation. Use for MDR compliance assessment, classification decisions, technical file preparation, and regulatory requirement interpretation.
Senior QMS Audit Expert for internal and external quality management system auditing. Provides ISO 13485 audit expertise, audit program management, nonconformity identification, and corrective action verification. Use for internal audit planning, external audit preparation, audit execution, and audit follow-up activities.
Senior CAPA Officer specialist for managing Corrective and Preventive Actions within Quality Management Systems. Provides CAPA process management, root cause analysis, effectiveness verification, and continuous improvement coordination. Use for CAPA investigations, corrective action planning, preventive action implementation, and CAPA system optimization.
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.