7TH SEMI-ANNUAL DEVICE AND DIAGNOSTIC LABELING CONFERENCE June 26–27, 2017 | San Jose, CA DOWNLOAD AGENDAREGISTER NOW ; Home Day One Day Two Registration Speakers Sponsors Attendees Hotel Register Today Add to Calendar Special Thanks to Our Sponsors Optimizing...
7TH SEMI-ANNUAL DEVICE AND DIAGNOSTIC LABELING CONFERENCE June 26–27, 2017 | San Jose, CA DOWNLOAD AGENDAREGISTER NOW ; Home Day One Day Two Registration Speakers Sponsors Attendees Hotel Register Today Add to Calendar Special Thanks to Our Sponsors Optimizing...
In a new article from MDDIonline.com, “FDA rules require medical device labelers to submit data to the Global Unique Device Identification Database (GUDID) for the highest-risk medical devices and will soon expand to moderate risk (Class II) devices in September...
