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Author Info

Marc Chaillou

Marc Chaillou

Head of Sales Europe and Global Strategic Projects, Schlafender Hase
Marc Chaillou is Head of Sales Europe and Global Strategic Projects at Schlafender Hase. He has been working for the Pharmaceutical & Medical Devices industries since 2011. Marc specialises in prepress labelling and specifically how processes & technologies can reduce costs and delays, increase efficiencies while reinforcing patient and consumer safety.  Marc has also worked in the Fast-Moving Consumer Goods industry.
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Marc Chaillou

Navigating Medical Device Regulations: How to Meet Labeling Artwork Compliance Standards

May 8, 2024

4 minutes read

Navigating Medical Device Regulations: How to Meet Labeling Artwork Compliance Standards

The medical devices regulations (MDRs) were introduced to take account of scientific and technological advances over the past two decades, but also due to problems interpreting previously existing regulations.

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Proofreading Software: 6 Savings in 2024

January 16, 2024

4 minutes read

Proofreading Software: 6 Savings in 2024

Comparison software offers immense savings, especially in regulated industries. Ask some of the leading pharmaceutical companies. Here are 6 Ways You Save.

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9 Reasons Proofreading in Life Sciences Can Be a Nightmare

October 2, 2023

3 minutes read

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 proofreading in life sciences can be a nightmare.

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8 Secrets Proofreaders Don’t Want to Reveal

March 25, 2022

3 minutes read

8 Secrets Proofreaders Don’t Want to Reveal

First, by proofreading, we mean text comparison of 2 files, like a manuscript versus a laid-out artwork of what should be the same text, not content correction of a single text. Over the years, many proofreaders have shared with us what manual text comparison really means for them. When they try to convince their boss to invest in electronic text comparison software, they usually present the business reasons, discussing ROI, risk avoidance, improved quality, time savings and so on.

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What Bill Murray and Text Comparison Have in Common

February 21, 2022

2 minutes read

What Bill Murray and Text Comparison Have in Common

Ready to put an end to repetitive correction cycles?

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Understanding Unicode for Proofreaders

November 17, 2021

4 minutes read

Understanding Unicode for Proofreaders

Unicode is a computer and software industry standard for handling text. While it is possible to geek-out on the technical aspects of Unicode (and if you’re so inclined you can check out the Wikipedia page on Unicode and the Unicode Consortium website), in this article we’re going to focus more on understanding the fundamentals, and discuss why this basic knowledge is critical for anyone who is part of a document creation / editing / review / correction workflow in a highly regulated industry.

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Live vs. Rasterized vs. Vectorized Text

October 20, 2021

4 minutes read

Live vs. Rasterized vs. Vectorized Text

In a previous post, we covered the basics of Unicode and why it’s so important for proofreaders (or anyone involved in the document creation, review and correction workflow) to understand the differences between the way humans and computers read language. Today, we’ll build on that knowledge as we examine different ways design and print proofs can be exported to PDF and the risks associated with removing live text from your organization’s documents.

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Common Labeling Errors That  Lead to Pharmaceutical Recalls

October 12, 2021

4 minutes read

Common Labeling Errors That Lead to Pharmaceutical Recalls

Explore the impact of labeling errors on pharmaceutical recalls. Find out how to avoid these mistakes and maintain compliance with industry regulations.

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MDR e-Labeling

October 6, 2021

2 minutes read

MDR e-Labeling

The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.

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MDR Graphic Symbols

October 6, 2021

2 minutes read

MDR Graphic Symbols

Over the last few posts, we have been touching upon different labelling requirements set by the MDR.

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September 2, 2024

Schlafender Hase Team

Avalis Publishing Case Study – Compliance through Watertight Version Control

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

September 2, 2024

Schlafender Hase Team

Soaring Medical Device Scrutiny: How is the Market Adapting?

4 minutes read

Soaring Medical Device Scrutiny: How is the Market Adapting?

August 22, 2024

Schlafender Hase Team

FHIR: Transforming Product Labeling

The shift from paper-based to digital processes has opened enormous opportunities in the healthcare sector in terms of data sharing and content management. But data can only be shared efficiently and add value if systems can "talk" to each other. The term we use for how compatibly systems work together is "interoperability." Traditionally, the healthcare sector has suffered from a high lack of interoperability.

6 minutes read

FHIR: Transforming Product Labeling

The shift from paper-based to digital processes has opened enormous opportunities in the healthcare sector in terms of data sharing and content management. But data can only be shared efficiently and add value if systems can "talk" to each other. The term we use for how compatibly systems work together is "interoperability." Traditionally, the healthcare sector has suffered from a high lack of interoperability.