Author Info

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

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

May 22, 2025

< 1 minute read

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.

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April 11, 2025

3 minutes read

Automating The Artwork Review Process

Speed to market is king in the fast-moving world of consumer goods. Yet, countless hours are spent reviewing packaging artwork before going to market. Traditional review methods are time-consuming and prone to human error. A single mistake in an ingredient list or a barcode could result in lost sales or shelf space, a recall and damage to the brand reputation.

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Ensure Compliance with the Latest Cosmetic Trends and Regulations

March 7, 2025

5 minutes read

Ensure Compliance with the Latest Cosmetic Trends and Regulations

As cosmetic regulations evolve, maintaining labeling standards is becoming increasingly complex. Here we explore some key changes in cosmetic labeling regulations and highlight how to ensure your products meet all requirements.

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Regulatory Changes and Compliance in the Agrochemical Industry

October 18, 2024

5 minutes read

Regulatory Changes and Compliance in the Agrochemical Industry

Agrochemicals are vital for improving farming efficiency. They include key products like pesticides, herbicides, and fertilizers, which help farmers boost crop yields and protect against pests. In order to minimize environmental and health risks, strict regulations govern the agrochemical industry.

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How to Prepare Product Labeling for an EPA Label Review

October 7, 2024

5 minutes read

How to Prepare Product Labeling for an EPA Label Review

The U.S. Environmental Protection Agency (EPA) label review process plays a crucial role in ensuring that pesticide products are used safely and effectively. These product label reviews are an essential part of the regulatory process before a pesticide can be registered and marketed.

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Understanding Document Comparison Software: A Key Tool for Regulatory Affairs in Crop Science

September 27, 2024

4 minutes read

Understanding Document Comparison Software: A Key Tool for Regulatory Affairs in Crop Science

Much like in the pharmaceutical and medical device sectors, where the adoption of such software has proven to reduce workloads and the risk of errors that may cause recalls or stop-sales, the Crop Science industry is also beginning to recognize the value of integrating this technology.

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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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January 16, 2024

4 minutes read

Proofreading Software: 6 Ways You Save

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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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.

5 minutes read

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

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?

2 minutes read

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

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.

2 minutes read