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Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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.

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

eBooks

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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.

eBooks

SEE ALL eBooks

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

SEE ALL BLOGS

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

SEE ALL Case Studies

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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.

SEE ALL Press Releases

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

Webinars

January 17, 2024

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. 

SEE ALL webinars

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

eBooks

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

SEE ALL eBooks

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

SEE ALL BLOGS

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

SEE ALL Case Studies

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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.

SEE ALL Press Releases

Videos

The Never-Ending Leaflets

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

Webinars

January 17, 2024

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. 

SEE ALL webinars

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Webinars

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. 

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Blogs

March 22, 2024

Schlafender Hase Team

Best Practices for your Promotional Review Process

The aim of a pharmaceutical promotional review process is to ensure the accuracy and compliance of promotional material with the relevant medical, legal, and regulatory aspects of a specific market.

March 18, 2024

Schlafender Hase Team

Ensuring Patient Safety: Medical Device Recall Process and Prevention Strategies

The costs of medical device recalls can run well into the millions of dollars. In terms of numbers of devices recalled, heading the unfortunate list of medical device recalls in recent times is a Class I recall of 38 million Vial2Bag fluid transfer systems by West Pharmaceuticals in 2019.

February 15, 2024

Schlafender Hase Team

Proofreading Regulated Documents in Pharma

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Case Studies

January 10, 2024

Schlafender Hase Team

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.

June 19, 2023

Schlafender Hase Team

Freyr Solutions Case Study- Achieving Ambitious Growth Targets with TVT

After implementing TVT, Freyr Solutions found the document authentication it sought, and saved time. This has been important to its continued growth trajectory.

June 8, 2023

Schlafender Hase Team

Dr. Max Pharma Case Study – Keeping the Devil Out of the Details

How Dr. Max Pharma Artwork Development teams saved time, increased accuracy and achieved greater confidence creating and verifying artwork for labeling and packaging in the pharmaceutical industry. Automated proofreading unleashed new capabilities and fostered team spirit.

Press Releases

November 7, 2023

Schlafender Hase Team

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.

June 27, 2023

Schlafender Hase Team

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.

November 8, 2022

Schlafender Hase Team

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

September 15, 2023

Schlafender Hase Team

A Buyer’s Guide to Purchasing Proofreading Software

Have you identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

March 7, 2023

Schlafender Hase Team

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors

March 6, 2023

Schlafender Hase Team

E-Labelling: Practical Next Steps for Medical Device Manufacturers

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

Publications

June 5, 2023

Schlafender Hase Team

How to Transition to E-Labelling – Practical Next Steps

E-labelling provides patients and healthcare professionals with up-to-date product and safety information. Schlafender Hase’s Dr. Jutta M. Hohenhörst discusses the benefits of e-labelling for the medical device sector and provides some practical tips for getting ahead with processes, procedures and solutions that deliver efficiencies across today’s labelling landscape, and add value for patients.

May 4, 2023

Schlafender Hase Team

Introducing e-Labelling For Medical Devices

In the consumer world, it’s now common practice to access product information online. For detailed instructions or information about manufacturing practices, safety advice and so on, users can scan a QR code or go to a web address. This will take them to the latest details, in an easily digestible format – often including audio and video options now, for maximum accessibility.

April 19, 2023

Schlafender Hase Team

Preparing for a Paperless Future: How the Medical Device Sector is Embracing e-labelling

As the medical device sector continues to rapidly evolve, it is becoming increasingly important to ensure that patients and healthcare professionals have access to up-to-date product and safety information. E-labelling provides a convenient way to share important information. Here, Schlafender Hase’s Peter Muller explores the advantages of e-labelling for the medical device sector, as well as providing some practical tips for getting ahead with the processes, procedures and solutions necessary for a successful transition to e-labelling.