This workshop is designed as an essential resource for professionals engaged in the oversight of FDA-regulated drugs, biologics, and medical devices.
By employing a multifaceted educational approach that includes pre-learning modules, hands-on exercises, and real-world case studies, the workshop aims to equip attendees with the skills necessary to navigate the complex landscape of FDA regulations for the conduct of research with human subjects effectively. The instructional content will address a range of critical aspects of FDA regulations, from legal frameworks and compliance protocols to specific challenges associated with emerging technologies.
Learning Objectives