Total 52,033 skills, Security & Compliance has 2053 skills
Showing 12 of 2053 skills
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.
Investigate an email address — validate it, find linked accounts and breaches, and pivot to the owner's identity, usernames, and other contact selectors.
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.
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.
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.
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.
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.
Initialize and manage the evidence collection directory for professional security audits with documented proof of findings.
Add Clerk authentication to any project by following the official quickstart guides.