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Blogs

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.

3 minutes read

Rising regulatory demands: are medical device suppliers ready?

The global medical devices market is set to reach $886.80 billion in value by 2032 . As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing.

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.

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® 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.

2 minutes read

Schlafender Hase® releases TVT version 11 with more power and enhanced user-friendliness

Schlafender Hase® today announced the release of TVT 11, a new version of its industry-leading proofreading software.

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 Regulatory Requirements for Medical Devices

Peter Muller & Mike Baird of Schlafender Hase how well they think suppliers are adapting to new regulatory demands for Class 2 and 3 Medical Device Manufacturers.

4 minutes read

The booming medical device sector: How well are suppliers adapting to new regulatory demands?

4 minutes read

Soaring Medical Device Scrutiny: How is the Market Adapting?

Webinars

Schlafender Hase Team

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

< 1 minute read

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

2 minutes read

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

2 minutes read

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

Blogs

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.

3 minutes read

Rising regulatory demands: are medical device suppliers ready?

The global medical devices market is set to reach $886.80 billion in value by 2032 . As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing.

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.

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® 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.

2 minutes read

Schlafender Hase® releases TVT version 11 with more power and enhanced user-friendliness

Schlafender Hase® today announced the release of TVT 11, a new version of its industry-leading proofreading software.

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 Regulatory Requirements for Medical Devices

Peter Muller & Mike Baird of Schlafender Hase how well they think suppliers are adapting to new regulatory demands for Class 2 and 3 Medical Device Manufacturers.

4 minutes read

The booming medical device sector: How well are suppliers adapting to new regulatory demands?

4 minutes read

Soaring Medical Device Scrutiny: How is the Market Adapting?

Webinars

Schlafender Hase Team

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

< 1 minute read

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

2 minutes read

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

2 minutes read

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

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

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.

3 minutes read

Rising regulatory demands: are medical device suppliers ready?

The global medical devices market is set to reach $886.80 billion in value by 2032 . As devices become more critical to patient outcomes, regulators’ quality and safety expectations and associated controls are increasing.

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.

Press Releases

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.

2 minutes read

Schlafender Hase® releases TVT version 11 with more power and enhanced user-friendliness

Schlafender Hase® today announced the release of TVT 11, a new version of its industry-leading proofreading software.

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 Regulatory Requirements for Medical Devices

Peter Muller & Mike Baird of Schlafender Hase how well they think suppliers are adapting to new regulatory demands for Class 2 and 3 Medical Device Manufacturers.

4 minutes read

The booming medical device sector: How well are suppliers adapting to new regulatory demands?

4 minutes read

Soaring Medical Device Scrutiny: How is the Market Adapting?

Webinars

Schlafender Hase Team

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

< 1 minute read

The Role of Barcodes in Life Sciences, and the Key to Ensuring Barcode Accuracy

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

2 minutes read

Embracing e-Labeling in a global context

As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

2 minutes read

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term “Artificial Intelligence” will be discussed, and which might be desirable in a given context. 

Press Releases

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.