The world's leading automated proofreading software

Proofreading

October 2, 2023

Schlafender Hase Team

9 Reasons Proofreading in Life Sciences Can Be a Nightmare

Risks, stress and more – there’s a lot at stake when you proofread in regulated industries. Here are nine reasons why.

August 23, 2023

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

June 28, 2023

Schlafender Hase Team

5 Ways a Proofreading Software will Keep your Regulatory Affairs Team Happy

Proofreading documents manually in regulatory affairs (RA) in the life sciences industry is stressful, high-risk and can lead to job dissatisfaction. The stakes are high – errors can harm patient health, result in product recalls, and damage brand and company reputations. Here’s how TVT, the proofreading software for regulatory affairs, can keep an RA team happy.

June 27, 2023

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

May 26, 2023

Schlafender Hase Team

Unlocking the True Value of a Document Comparison Software

Join Schlafender Hase as we discuss the challenges faced by life science companies when it comes to ensuring the accuracy of all digital and printed material and how technology can play an integral role in improving this process.

May 5, 2023

Schlafender Hase Team

RAPS Sponsored Webcast: The Foundations of AI: A Non-Technical Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile, Health Authorities are looking to regulate the use of AI. As a regulatory affairs professional, it is essential to have an understanding of this technology. In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context.

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software For Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

December 13, 2022

Schlafender Hase Team

10 Reasons Top Pharma Companies Automate Proofreading with TVT

Top pharma companies automate proofreading with TVT. Read all top 10 reasons.