Lisa Madison
Member since: Dec 23, 2024
Published articles: 1
What Are the Steps of the 510(K)-Submission Process?
People who want to market their either Class I or Class II device products in the U.S, and the device is not exempt from 510(k), must file a Premarket Notification with the FDA, it is also known as...
Articles > Reference & Education > Science
Dec 26, 2024
Author Bio
With the rapid development of the pharmaceutical industry, the importance of product safety and regulatory approvals are on the rise.