Introduction to the US FDA E-Learning with WMDO

This course examines the range of the US FDA’s responsibilities and provides a chronological history of significant events regarding the US FDA and medical devices. It lays the foundation by exploring the regulations found in 21 Code of Federal Regulations (CFR) and the various pathways of marketing medical devices in the US.

To enroll and purchase this course, please visit the WMDO website at: http://www.wmdo.org/SGS.aspx

Upon successfully completing this course, learners will be able to:

• Gain a better understanding of the definition of the US FDA
• Grasp the US FDA’s current responsibilities within the medical device industry
• Recognize the history of the US FDA as it relates to the current regulation of medical devices