Enables algorithmic trading compliance with MiFID II Article 17, providing tools for strategy classification, RTS 6 testing, and best execution audits. Also supports EU AI Act compliance.
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.
An MCP server for regMD that provides global medical device regulatory intelligence across 15 jurisdictions. It enables users to classify devices, query regulatory alerts, and find market expansion pathways via agencies like the FDA and EU MDR.
Provides automated EU AI Act compliance tools, including risk classification, role determination, transparency disclosures, content watermarking, deepfake labeling, and security threat detection.