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Regulatory

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.

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 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.

November 3, 2022

Schlafender Hase Team

Introducing Text Verification Tool®

November 3, 2022

Schlafender Hase Team

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.

November 2, 2022

Schlafender Hase Team

Change Management

As they try to plug the gaps, and hang on to the qualified and experienced experts they already have, life sciences companies need to be clever about how they support those people to make best use of the time, and how they alleviate the aspects of their job which add the least value professionally yet cannot be skimped on.

October 20, 2022

Schlafender Hase Team

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.

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

September 22, 2022

Schlafender Hase Team

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.