UDI Perspectives and Timetables Explained by FDA Senior Advisor in Recent Article
This is an important update to the Food and Drug Administration’s (FDA) timelines for UDI (Unique Device Identification) implementation deadlines. It comes by way of a recently published article entitled, “The FDA’s Take on Unique Device Identification,” authored by Jay Crowley who is senior advisor for patient safety for the Food and Drug Administration’s Center for Devices...
A ground-breaking white paper: Compliance with UDI Labeling Mandates: A Proven Methodology
We have a brand new and very compelling White Paper just out. Compliance with UDI Labeling Mandates: A Proven Methodology, was produced because, as the introduction states: There has never been a better or more urgent time for manufacturers of healthcare products to make a close examination of their product labeling systems. If you read...
GHS and Regulatory Labeling Challenges in the New Era 
