#Barnett
Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.
Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).
Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.
Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.
Archive: Introduction to the FDA
Course Description
This course begins with a comprehensive overview of FDA’s entire organization, and then drills down into a review of the Drug, Biologic, and Medical Device Centers. We will look at how each center is organized, how each center functions, the types of submissions each center reviews, and how each center conducts the review process.
Video Preview
Learning Objectives
- Discuss general information about FDA
- Detail the functions of the Center for Drug Evaluation and Research (CDER)
- Detail the functions of the Center for Biologics Evaluation and Research (CBER)
- Detail the functions of the Center for Devices and Radiological Health (CDRH)
- Discuss the types of submissions each FDA center reviews
Who Should Attend
- This course is appropriate for those who require a general introduction to FDA and how the FDA centers function, and professionals new to the industry that require an introduction to basic FDA information and are in Regulatory Affairs, Clinical, Quality, Manufacturing, Research, Legal, and other departments.
Instructor
Albert A. Ghignone, M.S., R.A.C.
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.