A multinational medical device company. The client needed to generate the application documents required for medical device compliance submissions.
Using large language models, the assistant understands user requirement documents, parses document specifications, generates structured content, and produces written text aligned to the required standard. It integrates an authoritative RAG knowledge base with multilingual processing, and can automatically search, translate and distil journal literature and experimental reports to support evidence- based writing. Output supports Word formatting and allows for subsequent manual review and revision. The agent automatically breaks down complex task objectives and dynamically schedules the various tool modules.