概要
This skill automates the complex process of designing clinical trials by integrating real-time data from clinical trial registries and FDA databases. It employs a modular, waypoint-based architecture that guides users from initial intervention research and regulatory pathway identification through to statistical sample size calculations and the generation of NIH-standard protocol documentation. By leveraging specialized MCP servers and Python-based statistical scripts, it ensures that intervention designs are grounded in existing research and meet the rigorous requirements of regulatory submissions for investigational products.
