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Philipp Thomas

Philipp Thomas

Account Executive, Schlafender Hase
Philipp Thomas is a dedicated Account Executive, helping proofreaders in Regulatory Affairs and Labeling to ensure accuracy and compliance. With expertise in the TVT – Text Verification Tool, Philipp helps prevent recalls due to labeling errors, reduces time and risk, increases labeling compliance, and avoids overlooked deviations.
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Philipp Thomas

The Future of Patient Information: A Discussion on GI 4.0® with Manuela Wiegand from Rote Liste

March 11, 2025

4 minutes read

The Future of Patient Information: A Discussion on GI 4.0® with Manuela Wiegand from Rote Liste

The way patients access critical medication information is evolving. In this expert discussion, Philipp Thomas from Schlafender Hase speaks with Manuela Wiegand, pharmacist at Rote Liste® Service GmbH, about Gebrauchsinformation 4.0 (GI 4.0®)—Germany’s move toward digital patient information leaflets.

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How To Ensure Your Labels Are Always Compliant

October 16, 2023

4 minutes read

How To Ensure Your Labels Are Always Compliant

Labeling compliance is important. Find out why, and discover how you can ensure your product labeling is compliant with regulations for pharmaceutical and food products.

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

July 31, 2023

4 minutes read

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?

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What is Document Comparison Software For Regulatory Affairs?

March 15, 2023

5 minutes read

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.

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8 Ways RA can help get Products to Market Faster

March 2, 2023

5 minutes read

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.

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10 Automated Proofreading Benefits that Make Your Life Easier

September 8, 2022

4 minutes read

10 Automated Proofreading Benefits that Make Your Life Easier

Whether you proofread labeling and packaging full-time, or proofreading is just one of your many tasks in your working day, automated proofreading with TVT, the Text Verification Tool©, will make your life easier.

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Mot.Tiff Case Study – Quality, Traceability and Right First Time with TVT

August 23, 2022

5 minutes read

Mot.Tiff Case Study – Quality, Traceability and Right First Time with TVT

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

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Are You Struggling to Proofread Foreign Languages or Braille?

June 21, 2022

4 minutes read

Are You Struggling to Proofread Foreign Languages or Braille?

“A different language is a different vision of life,” said the Italian film director, Federico Fellini.

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Manual vs Automated Proofreading

June 10, 2022

3 minutes read

Manual vs Automated Proofreading

When was the last time you flew in a passenger jet? Would you have felt as safe if the jet didn’t have automated controls? These relieve pilots of repetitive actions, reducing the risk of error and allowing pilots to focus on broader tasks related to safety and operation.

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Top 8 Causes of PDF Artwork Mistakes: How to Avoid Errors in Labeling and Design

August 25, 2021

3 minutes read

Top 8 Causes of PDF Artwork Mistakes: How to Avoid Errors in Labeling and Design

As you can see, the way in which the graphic designer / typesetter works as well as the tools and processes they use will influence the quality and content of the PDF Artwork.

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How FMCG and CPG Companies Can Improve Regulatory Risk Management for Packaging

June 12, 2025

Schlafender Hase Team

How FMCG and CPG Companies Can Improve Regulatory Risk Management for Packaging

In the rapidly changing and highly competitive Fast-Moving Consumer Goods (FMCG) sector, labeling and packaging plays an important role in brand identity, over and above its purpose of protecting the physical product.

How FMCG and CPG Companies Can Improve Regulatory Risk Management for Packaging
  • June 12, 2025
  • By: Vineed Ravindranath
5 minutes read

How FMCG and CPG Companies Can Improve Regulatory Risk Management for Packaging

In the rapidly changing and highly competitive Fast-Moving Consumer Goods (FMCG) sector, labeling and packaging plays an important role in brand identity, over and above its purpose of protecting the physical product.

E-labeling and what it means for regulatory teams

May 29, 2025

Schlafender Hase Team

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

E-labeling and what it means for regulatory teams
  • May 29, 2025
  • By: Schlafender Hase
2 minutes read

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

Press Release Cloud Native TVT

May 28, 2025

Schlafender Hase Team

Schlafender Hase Brings Pharma-Level content review and compliance to the CPG Industry with a new cloud-native version of TVT

TVT, Schlafender Hase’s flagship software, has long been the trusted standard for document and label review in the pharmaceutical industry. The new cloud-native version builds on the same proven comparison engine at the core of the desktop product. With a responsive web interface, scalable microservices architecture, and standards-based RESTful APIs, it delivers enhanced flexibility, intuitive usability, and seamless integration with existing document and artwork management systems, making world-class quality control more accessible to CPG teams.

Press Release Cloud Native TVT
  • May 28, 2025
  • By: Schlafender Hase
2 minutes read

Schlafender Hase Brings Pharma-Level content review and compliance to the CPG Industry with a new cloud-native version of TVT

TVT, Schlafender Hase’s flagship software, has long been the trusted standard for document and label review in the pharmaceutical industry. The new cloud-native version builds on the same proven comparison engine at the core of the desktop product. With a responsive web interface, scalable microservices architecture, and standards-based RESTful APIs, it delivers enhanced flexibility, intuitive usability, and seamless integration with existing document and artwork management systems, making world-class quality control more accessible to CPG teams.


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