The world's leading automated proofreading software

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Schlafender Hase

Schlafender Hase

Document Comparison Software For Regulated Industries
Schlafender Hase delivers an easy-to-use software solution to reduce the time you spend proofreading. Our solution catches even the smallest deviation early in the process, drastically improving overall document quality. Serving regulated industries including Pharmaceutical, Medical Devices, Chemical, and Crop Science.
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Schlafender Hase

FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams

August 19, 2025

< 1 minute read

FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams

E-labeling is no longer on the horizon - it’s here. That’s why we created this playbook: a one-stop resource combining expert insights, survey data, and practical guidance for life sciences professionals.

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Schlafender Hase Announces Change in Executive Leadership

June 30, 2025

2 minutes read

Schlafender Hase Announces Change in Executive Leadership

Founder & Chief Executive Officer Frank Hessler to join advisory board; André Cerbe to continue as sole Chief Executive Officer, supported by a strong Leadership team including Chief Technology Officer Karthikeyan Pandiyan.

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

May 29, 2025

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?

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

May 28, 2025

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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Reducing Labeling Risks: Applying Pharma’s Compliance Playbook to Food Labeling, Upcoming Webinar Hosted by Xtalks

May 20, 2025

2 minutes read

Reducing Labeling Risks: Applying Pharma’s Compliance Playbook to Food Labeling, Upcoming Webinar Hosted by Xtalks

In this free webinar, learn why food labeling errors continue to happen despite existing processes. Attendees will gain insights into why labeling errors led to nearly half of food recalls in 2024 and what actionable steps can be taken to avoid food recall. The featured speakers will discuss which pharma’s best practices food manufacturers can apply to build stronger labeling standards to minimize compliance risks while increasing speed to market.

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Barcode Grading in a Digital World – A Guide for FMCG/CPG Industries

May 14, 2025

< 1 minute read

Barcode Grading in a Digital World – A Guide for FMCG/CPG Industries

How to Ensure Barcode Accuracy in a Fast-Moving Market: Barcodes are the backbone of traceability, compliance, and retail readiness. But in today’s digital-first design workflows, traditional print-based grading methods no longer tell the full story.

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Preparing for FHIR-based ePI – How a Proofreading Solution Supports your ePI Journey

May 12, 2025

< 1 minute read

Preparing for FHIR-based ePI – How a Proofreading Solution Supports your ePI Journey

As regulatory bodies move toward structured electronic product information (ePI) in FHIR XML format, life sciences organizations are under pressure to evolve. That includes how you verify and proofread content.

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E-labeling: The Road to Efficient Pharmaceutical Labeling and Packaging

January 13, 2025

< 1 minute read

E-labeling: The Road to Efficient Pharmaceutical Labeling and Packaging

Practical next steps for pharmaceutical manufacturers & distributors as regulators demand the digital delivery of customer-facing product information in place of paper inserts.

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Elevate Your Expertise with TVT e-Learning: Training for Precision and Professional Growth

December 5, 2024

2 minutes read

Elevate Your Expertise with TVT e-Learning: Training for Precision and Professional Growth

When you work in a regulated industry where the risk of mistake is high, staying proficient with your tech stack and compliant with evolving standards is essential. With TVT being a cornerstone for many professionals in document review and labeling accuracy, Schlafender Hase has introduced a comprehensive e-Learning portal.

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Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

November 19, 2024

2 minutes read

Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

Schlafender Hase announced today the release of TVT 12, the latest annual update to its industry-trusted proofreading software. This upgrade offers significant improvements on the current version TVT 11.1 based entirely on customer consultation and feedback.

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FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams

August 19, 2025

Schlafender Hase Team

FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams

E-labeling is no longer on the horizon - it’s here. That’s why we created this playbook: a one-stop resource combining expert insights, survey data, and practical guidance for life sciences professionals.

FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams
< 1 minute read

FHIR-Based ePI: A Practical Playbook for Regulatory and Labeling Teams

E-labeling is no longer on the horizon - it’s here. That’s why we created this playbook: a one-stop resource combining expert insights, survey data, and practical guidance for life sciences professionals.

From Review Bottlenecks

August 18, 2025

Schlafender Hase Team

From Review Bottlenecks to Business Gains: How TVT Transforms Content Verification Across Regulated Industries

In regulated industries, content verification has become a business-critical function. Regulatory scrutiny is increasing. Product portfolios are growing. Content is more complex and multilingual than ever before.

From Review Bottlenecks
3 minutes read

From Review Bottlenecks to Business Gains: How TVT Transforms Content Verification Across Regulated Industries

In regulated industries, content verification has become a business-critical function. Regulatory scrutiny is increasing. Product portfolios are growing. Content is more complex and multilingual than ever before.

Proofreading in Highly Regulated Industries

August 18, 2025

Schlafender Hase Team

Every Detail Matters: Proofreading in Highly Regulated Industries

In regulated industries like pharma, medical device, fast-moving consumer goods (FMCG), and crop science, documentation isn’t just part of the process — it is the process. It’s what stands between your product and the market, your team and regulatory approval, your brand and consumer trust.

Proofreading in Highly Regulated Industries
2 minutes read

Every Detail Matters: Proofreading in Highly Regulated Industries

In regulated industries like pharma, medical device, fast-moving consumer goods (FMCG), and crop science, documentation isn’t just part of the process — it is the process. It’s what stands between your product and the market, your team and regulatory approval, your brand and consumer trust.