Unique Device Identification

Covectra: Unit-Level Serialization
Machine Product Brief
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Covectra: Unit-Level Serialization

Entry-level serialization system for multiple industries offers affordability and enables regulatory compliance.
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44 Best Package Designs
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Progea’s Movicon SCADA system.
Feature Article
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Medical Devices Enter the Information Age

Despite increasing competitive and regulatory pressures, medical device manufacturers have an opportunity to seize a significantly growing market. Streamlining operations through automation will be key.
Medical devices
Controls Case Study
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Medical device firm wins with barcode labeling software

CFR enterprise barcode labeling software helps QTS reduce risk, increase efficiency, and become compliant with UDI and FDA 21 CFR Part 11 regulations.
HealthPack 2016 at the New Orleans' Astor Crowne Plaza.
News
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HealthPack accepting presentation abstracts for 2016 event through Aug. 24

Sterilization methods, UDI developments, test method validation among the topics sought by event team.
HealthPack 2016 at the New Orleans' Astor Crowne Plaza.
News
|

HealthPack accepting presentation abstracts for 2016 event through Aug. 24

Sterilization methods, UDI developments, test method validation among the topics sought by event team.
Unveiling Healthcare Packaging’s Top 10 online articles from 2014.
News
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Unveiling Healthcare Packaging’s Top 10 from 2014

Website visitors seek insights on market trends and forecasts, serialization, unique device identification, and the benefits of effective package design.
VIAL STOPPER. This image shows a continuous ink-jet code on a vial stopper.
Feature Article
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Comparing UDI and DSCSA coding

Although there are differences between the medical device Unique Device Identification (UDI) regulation and the Pharmaceutical Drug Supply Chain Security Act (DSCSA), Videojet Technologies’ Tim Kearns finds many common aspects across both.
New industry resource guides healthcare suppliers and providers in using GS1 standards in the context of recent regulation.
News
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GS1 Healthcare US releases implementation guideline for using GS1 standards to address FDA Unique Device Identification

New industry resource guides healthcare suppliers and providers in using GS1 standards in the context of recent regulation.
The audience during HealthPack 2013.
News
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HealthPack announces 2014 agenda

Medtronic’s Jackie Elkin will open the March 11-13 event in Albuquerque with a keynote address on unique product identification and medical device packaging.
TRAXSECURE UNALTERED. The TraxSecur™ security feature is printed, without a requirement for any special inks, as a background that looks similar to those seen on security paper, except that it is created as a unique “instance” relating to a single time and place, which inextricably links an individual package to its unique corresponding track-and-trace information; this is Serialized Security™.
Feature Article
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Update on serialization and unique device identification regulatory developments

Key regulatory developments could preempt California e-pedigree and provide clarity for manufacturers and packagers of pharmaceuticals, biologics, and medical devices.

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