The world's leading automated proofreading software

Author Info

Dr. Jutta Hohenhoerst

Dr. Jutta Hohenhoerst

Regional Sales Director, Schlafender Hase
Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business. She has experience in different departments from Supply Chain Management to Strategic Marketing in F. Hoffmann-La Roche HQ, AstraZeneca and Fresenius HQ. While working for IQVIA during 2005 and 2012 she broadened her knowledge through strategic consulting projects in the pharma, medical device and hospital sector.
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Dr. Jutta Hohenhoerst

Embracing e-Labeling in a global context

May 31, 2024

2 minutes read

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it's essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

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Sustainable Solutions: Enhancing Workflows through Paperless Document Reviews

April 8, 2024

4 minutes read

Sustainable Solutions: Enhancing Workflows through Paperless Document Reviews

Earth Day is a commitment to safeguarding and enhancing our natural environment, with an anticipated mobilization of over 1 billion people in 2024. At Schlafender Hase, when we thought about how Earth Day affected us as individuals and a company, we unanimously agreed: it's especially about trees and minimizing use of paper.

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How to Transition to E-Labelling – Practical Next Steps

June 5, 2023

4 minutes read

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses 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 across today’s labelling landscape, and add value for patients.

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Introducing e-Labelling For Medical Devices

May 4, 2023

5 minutes read

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format - often including audio and video options now, for maximum accessibility.

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

April 18, 2023

3 minutes read

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.

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Why Data Integrity is Important in Pharma

May 20, 2022

3 minutes read

Why Data Integrity is Important in Pharma

Learn about Data Integrity and its crucial role in maintaining valuable data for various stakeholders, including patients, communities, and companies, through ALCOA and ALCOA+ principles.

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Top 3 reasons to encourage your employees to participate in e-Learning

September 6, 2021

3 minutes read

Top 3 reasons to encourage your employees to participate in e-Learning

As part of our TVT e-Learning portal we are offering a free trial to anyone interested in getting a feel for the system.

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TVT Critical Word List Finds Common Proofreading Mistakes in Original Documents

June 2, 2021

2 minutes read

TVT Critical Word List Finds Common Proofreading Mistakes in Original Documents

by: Schlafender Hase

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Lohmann & Rauscher Case Study – More Output, Less Resources

September 16, 2020

3 minutes read

Lohmann & Rauscher Case Study – More Output, Less Resources

The return on investment was clear and rapid. “Errors were recognized quickly, and the number of correction cycles was significantly reduced,” said Michael Breiler, Lohmann & Rauscher’s Director of Packaging Development.

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Proofreading in the European Pharma Industry: Challenges and Misconceptions

March 11, 2020

2 minutes read

Proofreading in the European Pharma Industry: Challenges and Misconceptions

Eliminate your risk of misprints and perfect your pharma proofreading process by watching this webinar and using TVT.

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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
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
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
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.