Total 50,308 skills, Security & Compliance has 1966 skills
Showing 12 of 1966 skills
Find and review Google Drive files shared outside the organization.
Google Cloud Identity: Manage identity groups and memberships.
Google Workspace Alert Center: Manage Workspace security alerts.
List and review Google Workspace security alerts from Alert Center.
Compliance expert for snyk-agent-scan — the agent skill file scanner — NOT for other Snyk CLI tools (snyk test, snyk code SAST, snyk iac, snyk container). Fixes alerts through content restructuring, never by suppressing or deleting information. Covers every file in a skill directory: SKILL.md, references/, assets/, and any secondary markdown. Apply when authoring a new skill, editing an existing one, triaging a failed snyk-agent-scan run locally or in CI, or unblocking a PR held by agent scanner failures. Not applicable to dependency vulnerabilities, code security findings, or infrastructure misconfigurations — those are out of scope.
Add Clerk authentication to any project by following the official quickstart guides.
Authorization system with role-based access control. Must-have for all apps that manage personal or access-restricted data.
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.
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 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.