Total 52,534 skills, Security & Compliance has 2066 skills
Showing 12 of 2066 skills
Find internet-exposed hosts, services, and devices from third-party scan data. Use when searching Shodan or Censys, finding open ports and banners, identifying an IP's tech stack, or discovering exposed databases, cameras, or industrial devices — without scanning the target yourself.
Look up companies, officers, and ownership in official business registries and filings. Use when researching a company's legal entity, finding directors/shareholders/beneficial owners, checking incorporation records, or reading SEC/regulatory filings.
Mine GitHub, GitLab, and git history for people, infrastructure, and leaked secrets. Use when investigating a developer or org on GitHub, finding leaked API keys or credentials in code, or pivoting from commits, emails, and repos.
Discover subdomains and related domains from public TLS certificate logs. Use when enumerating subdomains, finding hidden or staging hosts, mapping an org's domains via crt.sh or Certificate Transparency, or spotting newly issued certificates.
Look up domain registration and DNS records. Use when running WHOIS/RDAP, querying DNS records (A, MX, TXT, NS, SPF, DKIM, DMARC), finding a domain's registrant, nameservers, or mail setup, or resolving IPs and ASNs.
Pentest a web app, API, codebase, repository, URL, domain, or IP with Strix — autonomous AI penetration testing that exploits and proves vulnerabilities (OWASP Top 10 and beyond — injection, XSS, SSRF, auth/access-control flaws, IDOR, business logic) instead of just flagging them. Runs self-hosted with the open-source CLI or via the managed app.strix.ai cloud, and returns validated findings with proof-of-concept exploits (Markdown, JSON, CSV, SARIF). Use when the user asks to pentest, hack, security-scan, security-audit, or find vulnerabilities in an app, API, website, or repo.
Fix security vulnerabilities found by a Strix pentest (open-source CLI or app.strix.ai cloud) — triage by severity, patch the root cause rather than the symptom, and re-run Strix to prove each fix actually closes the exploit. Handles injection, XSS, SSRF, broken access control, IDOR, and other validated findings. Use after a Strix scan reports findings, or when the user asks to remediate, patch, or fix security issues from a strix_runs report, vulnerabilities.json, findings.sarif, or a cloud scan.
Security-first vetting for OpenClaw skills. Use before installing any skill from ClawHub, GitHub, or other sources. Checks for red flags, permission scope, and suspicious patterns.
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.
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 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.
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.