FDA's Unique Device Identification (UDI) System: <--- follow this link to the FDA's free video
"FDA has issued a proposed rule on the establishment of a Unique Device Identification System. This system would require most medical devices distributed in the U.S. to carry a Unique Device Identifier (UDI). This system, comprised of the UDI code, application of the UDI to device labeling and packaging, and a related database, is designed to provide a standardized way to identify devices across all information sources and systems, including electronic health records and devices registries."
'via Blog this'
Return Home: The Health, Drug, Prescription, and GMP Supersite Blog
SkillsPlus Intl Inc. - The best GMP training, best QSR training, best instructors
SkillsPlus Intl Info Blog
The Health, Drug, Prescription, and GMP Supersite Gift Store
Shameless Plug — Dechert’s 2025 Life Sciences Day
47 minutes ago
No comments:
Post a Comment