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Blogs

2 minutes read

Introducing TVT 12: A New Era in Compliance and Efficiency

With growing demands on regulatory professionals to ensure accuracy and efficiency, the newest version of the industry-trusted proofreading software, TVT 12 delivers enhancements that allow users to navigate complex document requirements with greater ease and confidence.

4 minutes read

The Road Ahead: Exploring Regulatory Trends Shaping Med Device and Pharma in 2025

The life science industry is poised to undergo significant shifts, driven especially by new technologies in healthcare. Technologies are also driving greater transparency in supply chains. Other features of the industry landscape that we foresee for 2025 are a more globally harmonized regulatory framework.

2 minutes read

Schlafender Hase’s Customer-Led Development Process

Schlafender Hase follows a customer-led development process of continuously incorporating feedback from its users into every TVT upgrade.

Case Studies

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

3 minutes read

Tank Worldwide Case Study – Fast, focused quality control in advertising

The creative content from Tank WW includes text copy, videos, websites or micro-sites, email promotional material, PowerPoint presentations, and more. A proofreading team provides the quality control for advertising material to ensure accuracy, consistency and compliance across content and different media.

3 minutes read

Pharmanovia Case Study – Embracing Technology to Ensure Patient-Safety

When the specialty pharmaceuticals company Pharmanovia integrated TVT into its artwork workflow, it achieved new efficiencies and greater certainty.

Press Releases

2 minutes read

Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

2 minutes read

Schlafender Hase® Appoints André Cerbe as co-CEO, Paving the Way for International Growth

Schlafender Hase®, market leader in proofreading software for regulated industries, has announced that André Cerbe joins the company as co-CEO. He will work closely with the company’s founding CEO, Frank Hessler.

2 minutes read

Schlafender Hase® releases TVT version 11.1 with new functionalities for an e-labelling environment

Schlafender Hase® announced today the release of TVT 11.1, the latest version of its industry-leading proofreading software. Functionalities integrated into TVT 11.1 simplify text verification and workflows in an electronic labelling (e-labelling) environment, in which consumers and patients typically use mobile scanning and other technologies to access product information online, often via a smartphone app.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

eBooks

< 1 minute read

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.

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.

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.

Publications

4 minutes read

The Rise of Regulation: Can Compliance Strategies Keep Up?

Regulatory scrutiny of medical devices is increasing across developed economies to keep patients safe and maintain public confidence.

4 minutes read

The medical device sector’s surging regulatory burden: how are suppliers coping?

6 minutes read

Soaring Regulatory Demands in the Medical Device Sector: How Are Compliance Strategies Evolving?

As medical devices become more critical to patient outcomes, regulators around the world are steadily increasing controls around the manufacturing, distribution and monitoring of devices.

Webinars

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

Schlafender Hase Team

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

2 minutes read

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

Blogs

2 minutes read

Introducing TVT 12: A New Era in Compliance and Efficiency

With growing demands on regulatory professionals to ensure accuracy and efficiency, the newest version of the industry-trusted proofreading software, TVT 12 delivers enhancements that allow users to navigate complex document requirements with greater ease and confidence.

4 minutes read

The Road Ahead: Exploring Regulatory Trends Shaping Med Device and Pharma in 2025

The life science industry is poised to undergo significant shifts, driven especially by new technologies in healthcare. Technologies are also driving greater transparency in supply chains. Other features of the industry landscape that we foresee for 2025 are a more globally harmonized regulatory framework.

2 minutes read

Schlafender Hase’s Customer-Led Development Process

Schlafender Hase follows a customer-led development process of continuously incorporating feedback from its users into every TVT upgrade.

Case Studies

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

3 minutes read

Tank Worldwide Case Study – Fast, focused quality control in advertising

The creative content from Tank WW includes text copy, videos, websites or micro-sites, email promotional material, PowerPoint presentations, and more. A proofreading team provides the quality control for advertising material to ensure accuracy, consistency and compliance across content and different media.

3 minutes read

Pharmanovia Case Study – Embracing Technology to Ensure Patient-Safety

When the specialty pharmaceuticals company Pharmanovia integrated TVT into its artwork workflow, it achieved new efficiencies and greater certainty.

Press Releases

2 minutes read

Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

2 minutes read

Schlafender Hase® Appoints André Cerbe as co-CEO, Paving the Way for International Growth

Schlafender Hase®, market leader in proofreading software for regulated industries, has announced that André Cerbe joins the company as co-CEO. He will work closely with the company’s founding CEO, Frank Hessler.

2 minutes read

Schlafender Hase® releases TVT version 11.1 with new functionalities for an e-labelling environment

Schlafender Hase® announced today the release of TVT 11.1, the latest version of its industry-leading proofreading software. Functionalities integrated into TVT 11.1 simplify text verification and workflows in an electronic labelling (e-labelling) environment, in which consumers and patients typically use mobile scanning and other technologies to access product information online, often via a smartphone app.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

eBooks

< 1 minute read

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.

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.

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.

Publications

4 minutes read

The Rise of Regulation: Can Compliance Strategies Keep Up?

Regulatory scrutiny of medical devices is increasing across developed economies to keep patients safe and maintain public confidence.

4 minutes read

The medical device sector’s surging regulatory burden: how are suppliers coping?

6 minutes read

Soaring Regulatory Demands in the Medical Device Sector: How Are Compliance Strategies Evolving?

As medical devices become more critical to patient outcomes, regulators around the world are steadily increasing controls around the manufacturing, distribution and monitoring of devices.

Webinars

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

Schlafender Hase Team

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

2 minutes read

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

Case Studies

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

3 minutes read

Tank Worldwide Case Study – Fast, focused quality control in advertising

The creative content from Tank WW includes text copy, videos, websites or micro-sites, email promotional material, PowerPoint presentations, and more. A proofreading team provides the quality control for advertising material to ensure accuracy, consistency and compliance across content and different media.

3 minutes read

Pharmanovia Case Study – Embracing Technology to Ensure Patient-Safety

When the specialty pharmaceuticals company Pharmanovia integrated TVT into its artwork workflow, it achieved new efficiencies and greater certainty.

Blogs

2 minutes read

Introducing TVT 12: A New Era in Compliance and Efficiency

With growing demands on regulatory professionals to ensure accuracy and efficiency, the newest version of the industry-trusted proofreading software, TVT 12 delivers enhancements that allow users to navigate complex document requirements with greater ease and confidence.

4 minutes read

The Road Ahead: Exploring Regulatory Trends Shaping Med Device and Pharma in 2025

The life science industry is poised to undergo significant shifts, driven especially by new technologies in healthcare. Technologies are also driving greater transparency in supply chains. Other features of the industry landscape that we foresee for 2025 are a more globally harmonized regulatory framework.

2 minutes read

Schlafender Hase’s Customer-Led Development Process

Schlafender Hase follows a customer-led development process of continuously incorporating feedback from its users into every TVT upgrade.

Press Releases

2 minutes read

Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

2 minutes read

Schlafender Hase® Appoints André Cerbe as co-CEO, Paving the Way for International Growth

Schlafender Hase®, market leader in proofreading software for regulated industries, has announced that André Cerbe joins the company as co-CEO. He will work closely with the company’s founding CEO, Frank Hessler.

2 minutes read

Schlafender Hase® releases TVT version 11.1 with new functionalities for an e-labelling environment

Schlafender Hase® announced today the release of TVT 11.1, the latest version of its industry-leading proofreading software. Functionalities integrated into TVT 11.1 simplify text verification and workflows in an electronic labelling (e-labelling) environment, in which consumers and patients typically use mobile scanning and other technologies to access product information online, often via a smartphone app.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

eBooks

< 1 minute read

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.

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.

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.

Publications

4 minutes read

The Rise of Regulation: Can Compliance Strategies Keep Up?

Regulatory scrutiny of medical devices is increasing across developed economies to keep patients safe and maintain public confidence.

4 minutes read

The medical device sector’s surging regulatory burden: how are suppliers coping?

6 minutes read

Soaring Regulatory Demands in the Medical Device Sector: How Are Compliance Strategies Evolving?

As medical devices become more critical to patient outcomes, regulators around the world are steadily increasing controls around the manufacturing, distribution and monitoring of devices.

Webinars

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

Schlafender Hase Team

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

2 minutes read

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

Press Releases

2 minutes read

Schlafender Hase® Announces Upcoming Release of TVT 12 Proofreading Software

2 minutes read

Schlafender Hase® Appoints André Cerbe as co-CEO, Paving the Way for International Growth

Schlafender Hase®, market leader in proofreading software for regulated industries, has announced that André Cerbe joins the company as co-CEO. He will work closely with the company’s founding CEO, Frank Hessler.

2 minutes read

Schlafender Hase® releases TVT version 11.1 with new functionalities for an e-labelling environment

Schlafender Hase® announced today the release of TVT 11.1, the latest version of its industry-leading proofreading software. Functionalities integrated into TVT 11.1 simplify text verification and workflows in an electronic labelling (e-labelling) environment, in which consumers and patients typically use mobile scanning and other technologies to access product information online, often via a smartphone app.

Blogs

2 minutes read

Introducing TVT 12: A New Era in Compliance and Efficiency

With growing demands on regulatory professionals to ensure accuracy and efficiency, the newest version of the industry-trusted proofreading software, TVT 12 delivers enhancements that allow users to navigate complex document requirements with greater ease and confidence.

4 minutes read

The Road Ahead: Exploring Regulatory Trends Shaping Med Device and Pharma in 2025

The life science industry is poised to undergo significant shifts, driven especially by new technologies in healthcare. Technologies are also driving greater transparency in supply chains. Other features of the industry landscape that we foresee for 2025 are a more globally harmonized regulatory framework.

2 minutes read

Schlafender Hase’s Customer-Led Development Process

Schlafender Hase follows a customer-led development process of continuously incorporating feedback from its users into every TVT upgrade.

Case Studies

3 minutes read

Avalis Publishing Case Study – Compliance through Watertight Version Control

3 minutes read

Tank Worldwide Case Study – Fast, focused quality control in advertising

The creative content from Tank WW includes text copy, videos, websites or micro-sites, email promotional material, PowerPoint presentations, and more. A proofreading team provides the quality control for advertising material to ensure accuracy, consistency and compliance across content and different media.

3 minutes read

Pharmanovia Case Study – Embracing Technology to Ensure Patient-Safety

When the specialty pharmaceuticals company Pharmanovia integrated TVT into its artwork workflow, it achieved new efficiencies and greater certainty.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

eBooks

< 1 minute read

From Struggles to Solutions – Leveraging Technology for Faster Labeling Review in Crop Science

Across the Crop Science sector, both user and environmental safety are of highest priority. In this buyer’s guide, we will go over seven steps that will help you in your purchasing process, to ensure that you end up with the proofreading software you need.

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.

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.

Publications

4 minutes read

The Rise of Regulation: Can Compliance Strategies Keep Up?

Regulatory scrutiny of medical devices is increasing across developed economies to keep patients safe and maintain public confidence.

4 minutes read

The medical device sector’s surging regulatory burden: how are suppliers coping?

6 minutes read

Soaring Regulatory Demands in the Medical Device Sector: How Are Compliance Strategies Evolving?

As medical devices become more critical to patient outcomes, regulators around the world are steadily increasing controls around the manufacturing, distribution and monitoring of devices.

Webinars

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

Schlafender Hase Team

Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.

2 minutes read