Home Resource Center data Multimedia Videos Reclassifying MDDS From Class III to Class I: Impact On MDDS Manufacturers
Bookmark and Share

This is the resource

Video
Reclassifying MDDS From Class III to Class I: Impact On MDDS Manufacturers

Reclassifying MDDS From Class III to Class I: Impact On MDDS Manufacturers

 

On February 15th, 2011, the US FDA reclassified Medical Device Data Systems, or MDDS, from Class III to Class I with sweeping effects on MDDS manufacturers. This year, manufacturers must have quality management processes in place that are compliant with the more stringent requirements for Class I devices as defined in 21 CFR, Part 820. Find out what this means for you.

To view this video on YouTube, please click here.

To view the full On-Demand Webinar, please click here.



Document Actions