The world's leading automated proofreading software

Labeling

< 1 minute read

Swiss Cough Syrup Story

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Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

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Innovator Rx Drug Product Labeling: From Creation to Change Management

This webinar will help companies understand the nuances of global health authority drug product labeling requirements.

3 minutes read

Labelling Issues & Opportunities for UK Operators

This responsibility – to get everything right – often falls on Regulatory Affairs where the workload is high, and deadlines are short.

2 minutes read

Barocde Compliance: 3 Rules for Barcodes in Life Sciences

Optimize barcode scanning precision in pharmaceutical, artwork, quality control, packaging, and printing industries with these indispensable tips. Avoid delays and errors for smooth workflow.

12 minutes read

Reduce Labeling Errors in Your Artwork

Over the years, as we’ve worked to help make proofreading easier and more accurate for our customers, we’ve witnessed many different types of potential issues with labeling artwork design proofs. Most of these issues are visible to the human eye when reading through the document, but a few of them are invisible and require special techniques.

2 minutes read

Webinar: Make Sure Your Barcode Makes the Grade

In this webinar you will learn how TVT Barcode identifies barcode errors before they are printed and automatically detects, decodes, compares and grades barcodes used by highly regulated industries like Life Science.

2 minutes read

Schlafender Hase® Releases TVT Barcode

TVT Barcode is an add-on module that has been released with the new TVT® version 10.2. It has been designed for use across all industries, including the highly regulated pharmaceutical and medical devices industries.

4 minutes read

Common Labeling Errors That Lead to Pharmaceutical Recalls

Explore the impact of labeling errors on pharmaceutical recalls. Find out how to avoid these mistakes and maintain compliance with industry regulations.

2 minutes read

MDR e-Labeling

The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.