When you need to print a label, how long does it take to find the correct file, populate the correct data, and start the print job? If you’re not leveraging the power of variable data on smart label templates, it could take several minutes just to find the right label file!READ MORE
If you encountered a labeling error today, would you be able to confidently pinpoint how and why it took place? Unfortunately, for many companies, the answer is “no.” Many companies have a label design and approval process that is informal, manual, and prone to mistakes.
So, how can you reduce the risk of labeling errors to near zero? You can set your company up for success by implementing an automated label audit trail. A label audit trail is a reliable, consistent way of documenting changes made to label designs. Maintaining an accurate label audit trail reduces the risk of labeling errors and helps pinpoint the cause if they happen.READ MORE
Life sciences companies have a lot of factors to consider when it comes to labeling, including changes in regulations on an ongoing basis from authorities like the FDA and EU to protect public health and improve patient safety. This blog will go through global labeling regulations, compliance, labeling system validation, and labeling and artwork management solutions to support it all.READ MORE
When it comes to barcodes and their use on labels such as product, inventory, shipping, and case labels, quality is paramount. A poor-quality barcode label can result in delays in production, returns, chargebacks, poor customer experience, and potentially recalls – no company wants to face those headaches. Thankfully, there are many options and solutions to help improve the quality of barcode labels and safeguard your business’ labeling processes.READ MORE
According to the Enterprisers Project, security must be a top priority for technology executives in 2022. Building a secure barcode labeling process is an important piece of a company’s security strategy that has a direct impact on the bottom line.
Mislabeling is one of the top causes of recalls in the United States, and labeling errors stem from gaps in labeling security. This blog will discuss ways to create a managed, controlled, and secure barcode labeling process leveraging better connections between people, software, and process.READ MORE
Quality assurance (QA) is critical in manufacturing to ensure safety for employees and consumers of the product being manufactured. In highly-regulated industries like medical device manufacturing, pharmaceuticals, and life sciences, regulatory authorities like the United States Food & Drug Administration (FDA) and the European Union (EU) have guidelines related to process validation to confirm a company’s processes will result in reliable outputs and meet all necessary quality standards.READ MORE
Thermal printing is an extensively used and mature technology that is extremely reliable, but print issues can still occur when printing labels. Manufacturers depend on thermal printing for product identification, dosage information, voltage currents, use-by dates, batch information, model and serial numbers, to name a few.
By leveraging automatic label inspection technologies, you can inspect every label as it is printing and avoid critical labeling errors that can cost you time and money.READ MORE
Compliance labeling is critical for manufacturers and distributors in many industries. Managing compliance labeling doesn’t need to cause headaches when you use a robust and reliable enterprise labeling system. Following these key principles will set you up for compliance labeling success.READ MORE
How three different medical device companies implemented security and traceability into their labeling process.READ MORE
Integrating label printing systems with SAP is a guaranteed way to decrease labeling errors and maximize ROI while also speeding up your label printing process.READ MORE
The medical device industry is one of the most highly regulated industries out there.READ MORE
Lately, there’s been quite the buzz around the European Union Medical Device Regulation or better known as, EU MDR. The EU MDR is a priority for all companies in the medical device industry that distribute products in the EU and will officially take effect on May 26, 2021. This regulation has more need for data management and complex assessment procedures than the regulation it replaces (MDD – Medical Devices Directive).
Imagine a world without color - pretty boring, right?READ MORE
Imagine hand drawing floor plans for the Empire State Building before AutoCAD was developed; if you made a mistake, you often had to start from scratch, the process took forever, and the risk for errors was high.READ MORE
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