The world's leading automated proofreading software


January 10, 2024

Schlafender Hase Team

Pharmanovia Case Study – Embracing Technology to Ensure Patient-Safety

When the specialty pharmaceuticals company Pharmanovia integrated TVT into its artwork workflow, it achieved new efficiencies and greater certainty.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

April 18, 2023

Schlafender Hase Team

Reducing Medical Device Packaging Waste and Improving Information Provision Through E-Labelling

E-labelling offers patients and healthcare professionals the convenience of always having up-to-date information on their products, such as the latest safety updates. It also provides regulators with greater oversight and assurance that manufacturers are providing accurate and timely information. Dr. Jutta M. Hohenhörst, from Schlafender Hase, explores the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies and add value for patients.

March 13, 2023

Schlafender Hase Team

Azurity Pharmaceuticals Case Study – Effortless Comparison in Labeling and Promotional Review

Following an increase in the number of products after an acquisition, the labeling team at Azurity Pharmaceuticals encountered new challenges in their proofreading process. TVT was their chosen regulatory proofreading software.

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

Practical next steps for medical device manufacturers & distributors as regulators demand the digital delivery of customer-facing product information in place of paper inserts.

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we'll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives. 

January 31, 2023

Schlafender Hase Team

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.

January 13, 2023

Schlafender Hase Team

TVT Benefits Booklet

Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees' stress and ensured patient safety with an efficient proofreading workflow.