7 May–29 June 2018
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.
This virtual format offers a more flexible schedule, so you can take notes and review topics at your own pace, and includes six live Q&A sessions with regulatory experts who can provide more clarity and answer your specific questions. 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 following topic areas are covered:
- General information
- Medical devices
- Other product classifications
- Inspection and enforcement
This is a high-engagement program with different learning and study formats including:
- Eight weeks of lessons in a virtual classroom setting through on-demand webcasts
- Six live, expert-led Q&A sessions
- Expert regulatory facilitators
- Online community for virtual study groups
- RAC (US) practice exam
- Study checklist
- US exam content outline
At a Glance
Program Dates: 7 May – 29 June 2018
Registration Closes: 11 May 2018*
Refund Deadline: 30 April 2018
RAC Recertification Credits: None
Will the live Q&A webcasts be recorded? Yes
*Note: Access to the course content begins 30 April. Registrants after this date will be responsible for all assigned content that students are expected to cover prior to the first live Q&A Session on 22 May.