Foundations of US Medical Devices is an informative, full-day, expert-led program that helps you build a solid foundation of the regulatory competencies needed today. Take advantage of bonus content to expand your learning opportunity beyond the workshop.
During the program, you will learn the fundamentals of medical devices: QRS/QMS, design control, postmarket compliance, FDA inspections, and advertising, promotion and labeling.
In addition to the live, face-to-face program, we offer a special, blended learning opportunity with four online courses and relevant chapters from the just-released 9th edition of RAPS’ Fundamentals of US Regulatory Affairs.
Bonus materials include:
Online Course #1: Role of the Regulatory Professional
Online Course #2: Medical Devices: Definition & Lifecycle
Online Course #3: Medical Devices: US Regulations (Access will be granted during the program)
Online Course #4: Global Regulatory Strategy for Medical Devices (Access will be granted during the program)
Textbook: Selected medical device chapters from Fundamentals of US Regulatory Affairs (Access will be granted during the program)