The world's leading automated proofreading software

TVT

January 17, 2024

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI 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 affair 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. 

September 15, 2023

Schlafender Hase Team

A Guide to Purchasing Proofreading Software for Regulated Industries

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

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.

August 17, 2023

Schlafender Hase Team

A Guide to Medical Device Labeling Requirements

Navigating complex labeling requirements for medical devices. Your guide to the fundamentals of regulation and compliance and how automated proofreading can minimize your labeling risks.

July 31, 2023

Schlafender Hase Team

Maximizing the benefits of e-labeling in Pharma and Med Device

With electronic labeling gaining momentum across healthcare markets, are you ready to maximize the benefits?

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

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.

February 2, 2023

Schlafender Hase Team

13 Questions to Ask When Choosing Comparison Software

Settling on a text comparison solution that does not require you to change your existing processes can be a daunting task, but we are here to help! We’ve outlined 13 questions for you to ask before making your final choice.

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.

December 13, 2022

Schlafender Hase Team

The Never-Ending Leaflets