Review a contract against your organization's negotiation playbook — flag deviations, generate redlines, provide business impact analysis. Use when reviewing vendor or customer agreements, when you need clause-by-clause analysis against standard positions, or when preparing a negotiation strategy with prioritized redlines and fallback positions.
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.
Check the status of existing agreements with a vendor across all connected systems — CLM, CRM, email, and document storage — with gap analysis and upcoming deadlines. Use when onboarding or renewing a vendor, when you need a consolidated view of what's signed and what's missing (MSA, DPA, SOW), or when checking for approaching expirations and surviving obligations.
Explain recent changes and provide a structured summary with security checks
Contract & Proposal Writer
EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.
Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use for document control procedures, change control workflow, document numbering, version management, electronic signature compliance, or regulatory documentation review.
ISO 13485 Quality Management System implementation and maintenance for medical device organizations. Provides QMS design, documentation control, internal auditing, CAPA management, and certification support. Use when working with medical device quality systems, preparing for ISO 13485 audits, managing regulatory compliance documentation, setting up corrective actions, or building audit preparation programs. Useful for quality management, audit preparation, regulatory compliance, medical device documentation, and corrective action workflows.
Audit commits for issues and CHANGELOG entries
Conventional commit type keywords for PR titles and commit messages. Use when determining the change type for commits or PRs. Triggered by "what type", "label", "change type", "conventional commit", "t: label".
Audits game assets for compliance with naming conventions, file size budgets, format standards, and pipeline requirements. Identifies orphaned assets, missing references, and standard violations.
API — Tenancy — 17 abstractions. Tenant lifecycle and installation event handlers and use cases.
API — Tenant Manager — 2 abstractions. Tenant management event handlers and use 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.
Review Azure SDK management-plane pull requests, check naming conventions, API compatibility, and code quality.
Resolve review comments on Azure management-plane .NET SDK PRs. Handles renaming types/properties, changing property types, and other API surface adjustments by updating TypeSpec client.tsp and regenerating.
Review/generate third-party code attribution, licensing, and notice requirements
Create a new extension condition that controls when extensions are active. Use when you need to conditionally show or hide extensions based on application state (e.g., current section, user permissions, entity state, workspace context). Conditions are registered as extensions and referenced in manifest condition arrays.
Clarify requirements before implementing. Use when serious doubts arise.
Vulnerability remediation SLAs define mandatory timeframes for patching or mitigating identified vulnerabilities based on severity, asset criticality, and exploit availability. Effective SLA programs
