Regulatory Affairs 101 + Exercises
In this course, participants will learn about key regulatory concerns and requirements that they need to know as they design, develop, and test their devices. NEMIC will work with you to define your Med Tech products classification and create a framework to better understand your specific FDA submission requirements.
In this course, participants will learn about key regulatory concerns and requirements that they need to know as they design, develop, and test their devices. NEMIC will work with you to define your Med Tech products classification and create a framework to better understand your specific FDA submission requirements.
In this course, participants will learn about key regulatory concerns and requirements that they need to know as they design, develop, and test their devices. NEMIC will work with you to define your Med Tech products classification and create a framework to better understand your specific FDA submission requirements.
MedTech Mini: More About Regulatory Affairs 101
In this Med Tech Mini, NEMIC Virtual Classroom instructor Talia Serrecchia details what you'll learn during Regulatory Affairs 101.