Registration is open now for the RAC (US) Prep Virtual Program (Autumn 2017 Exam), beginning on 29 June 2017. The new virtual format offers a more flexible schedule, so you can take notes and review topics at your own pace, and includes eight live Q&A sessions with regulatory experts who can provide more clarity and answer your specific questions. A new on-demand webcast will be released on a different study area each week. Dig into and revisit topic areas you need more time on, or use familiar information as a reference to brush up on your regulatory knowledge.
The RAC (US) Prep Virtual Program provides a thorough knowledge of regulatory functions throughout product lifecycle for medical devices, IVDs, pharmaceuticals and biologics. Using the Fundamentals of US Regulatory Affairs book as a foundation, the program provides real-world examples and practical applications provided by regulatory experts. It also includes information about FDA regulations and employs critical thinking and analytical skills to help you better prepare for the RAC (US) exam.
The following topic areas are covered:
This is a high-engagement program with several learning and study formats including:
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
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