Electronic Labeling Encouraged In CDRH Blue Book Memo Outlining Means
This article was originally published in The Gray Sheet
Executive Summary
FDA is projecting that electronic labeling provisions in the Medical Device User Fee & Modernization Act could increase the number of devices that link to the Internet
You may also be interested in...
Pending Technical Corrections Put E-Labeling Guidance On Hold For Holidays
Additional electronic labeling guidance will await Congressional action on technical corrections to Sec. 206, according to FDA
Pending Technical Corrections Put E-Labeling Guidance On Hold For Holidays
Additional electronic labeling guidance will await Congressional action on technical corrections to Sec. 206, according to FDA
Professional-Use IVD E-Labeling Eligibility Supported By CDRH’s Phillips
A forthcoming FDA e-labeling draft guidance for prescription devices used in professional settings will include a broad definition of the term "healthcare facility," agency reps say