The world's leading automated proofreading software

Schlafender Hase Blue Logo
Book a demo

Home

Author Info

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.
Connect With Me!
Linkedin

Resources From

Schlafender Hase

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?

Read More!
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.

Read More!
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.

Read More!
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.

Read More!
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.

Read More!
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.

Read More!
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.

Read More!
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.

Read More!
Best Practices for Medical Device Label Management Compliance

August 8, 2024

2 minutes read

Best Practices for Medical Device Label Management Compliance

Managing medical device labels presents a myriad of challenges for manufacturers, including ensuring compliance with ever-evolving regulatory standards, maintaining accuracy and consistency in label content, and optimizing label design for clarity and usability.

Read More!
2024 Medical Device Compliance Strategies Research Report

August 8, 2024

3 minutes read

2024 Medical Device Compliance Strategies Research Report

As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing. But how well prepared are suppliers? We recently commissioned independent research to find out.

Read More!
FDA's New Front-of-Package Nutrition Labeling

June 26, 2025

Schlafender Hase Team

FDA’s New Front-of-Package Nutrition Labeling

The FDA's proposed front-of-package nutrition labeling represents one of the most significant food labeling changes in decades. This article introduces the proposed rule, countries that have already implemented it, and explores the economic and health benefits.

FDA's New Front-of-Package Nutrition Labeling
  • June 26, 2025
  • By: Dagmar Moreside
2 minutes read

FDA’s New Front-of-Package Nutrition Labeling

The FDA's proposed front-of-package nutrition labeling represents one of the most significant food labeling changes in decades. This article introduces the proposed rule, countries that have already implemented it, and explores the economic and health benefits.

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?


Facebook Linkedin Instagram Youtube
TVT e-Learning Portal

Schlafender Hase
Call: +49 69 24 44 810
Americas: +1 617 607 4900
Contact Us

TVT ® | Text Verification Tool ®

© 2025 Schlafender Hase Inc.

Book a Demo