What problem does it solve? Regulatory affairs professionals must manually monitor dozens of government websites across China, the EU, the US, and Canada to stay current on medical device regulations, guidance documents, recalls, and safety alerts—a time-consuming and error-prone weekly routine. ## Core Features & Use Cases - Multi-Region Scraping: Fetches updates from NMPA, CMDE, NIFDC, EC Health, MDCG, FDA CDRH, Health Canada, IMDRF, and Team NB using requests/BeautifulSoup, Playwright for JS-rendered pages, and AI web_fetch fallback for anti-crawler sources. - Deduplication & Reporting: Filters previously seen items with source+URL/title composite keys and generates a structured Markdown weekly report grouped by region with tags, dates, and compliance impact. - IMA Knowledge Base Upload: Automatically creates a note via the IMA OpenAPI and links it to the "MD法规更新汇总" knowledge base. - Use Case: Every Friday at 8:30, run the tracker to collect the past week's global regulatory updates, deduplicate them against local history, generate a weekly report, and push it to your IMA knowledge base. ## Quick Start Ask the AI to track this week's medical device regulatory updates and generate the latest weekly regulatory report.
