Enables management of software requirements in compliance with IEC 62304 Class C medical device standards, including requirement creation, versioning, traceability matrix generation, and risk control integration.
Manages backlog items and todos with status tracking, priorities, and dependencies. Stores work items as human-readable markdown files with automatic versioning.
Enables comprehensive software lifecycle management with structured tracking of requirements, tasks, and architecture decisions through an SQLite database with full traceability and automated state validation.
Enables multi-project workspaces to share structured notes, API contracts, and handoff messages via a local SQLite database, with versioning and read tracking.
Converts requirements into traceable, CI-ready Playwright BDD tests connected to business rules, with support for Gherkin generation, rule mapping, and automated test pipelines.
