Question
Penn Foster- Sterile Processing
Question: What is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class Ill medical devices called?
A. Premarket approval
B. Postmarket approval
C. Emergency use authorization
D. MedWatch
Question: What is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class Ill medical devices called?
A. Premarket approval
B. Postmarket approval
C. Emergency use authorization
D. MedWatch
Answers
GPT 3.5
A. Premarket approval