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Blogs

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 Ways You’re Wasting Time & Money in Regulatory Affairs

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we’ll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

SEE ALL BLOGS

Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

SEE ALL CASE STUDIES

Press Releases

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.

LexisNexis® Reed Tech™

April 26, 2022

Schlafender Hase Team

LexisNexis® Reed Tech™ and Schlafender Hase® Alliance Provides Mutual Customer Benefits for Pharmaceutical and Medical Device Companies

Founded in 2001, Schlafender Hase GmbH is headquartered in Frankfurt am Main, Germany, with a subsidiary in the US. More at: www.schlafenderhase.com

November 9, 2021

Schlafender Hase Team

Francisco Baraona Appointed Co-CEO of Schlafender Hase

Schlafender Hase has announced that Francisco Baraona joins the company as its co-CEO, effective November 1, 2021. He shares responsibility for operations with Frank Hessler, founding CEO of Schlafender Hase.

SEE ALL Press Releases

Videos

The Never-Ending Leafleats

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

eBooks

Med Device E-labelling

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives. 

Barcode grading e-book

January 31, 2023

Schlafender Hase Team

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.

Benefits of tvt

January 13, 2023

Schlafender Hase Team

TVT Benefits Booklet

Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees’ stress and ensured patient safety with an efficient proofreading workflow. 

SEE ALL eBooks

Publications

Medical Device Labelling

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

life sciences industry

November 2, 2022

Schlafender Hase Team

Change Management

As they try to plug the gaps, and hang on to the qualified and experienced experts they already have, life sciences companies need to be clever about how they support those people to make best use of the time, and how they alleviate the aspects of their job which add the least value professionally yet cannot be skimped on.

Routine Recall Risks

February 17, 2021

Schlafender Hase Team

The Devil in the Detail: 5 Routine Recall Risks Faced by Modern Pharma

With the steely eyes of the regulators firmly trained on everything that life sciences organisations do, the last thing firms want is to incur fines, market delays or worse because of overlooked mistakes in labelling and product information. Yet incidences of labelling issues and associated product recalls are rising sharply, now accounting for over 50% of all recalls according to the FDA. The conditions are rife for the trend to continue, due to growing complexity in life sciences firms’ operations and external market requirements.

SEE ALL Publications

Webinars

Digitizing Your Proofreading Workflow 

Schlafender Hase Team

Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

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.

Webinar: Level up with TVT 11

Schlafender Hase Team

Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

Webinar: e-PIL legislation

Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit. 

SEE ALL webinars

Blogs

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 Ways You’re Wasting Time & Money in Regulatory Affairs

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we’ll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

SEE ALL BLOGS

Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

SEE ALL CASE STUDIES

Press Releases

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.

LexisNexis® Reed Tech™

April 26, 2022

Schlafender Hase Team

LexisNexis® Reed Tech™ and Schlafender Hase® Alliance Provides Mutual Customer Benefits for Pharmaceutical and Medical Device Companies

Founded in 2001, Schlafender Hase GmbH is headquartered in Frankfurt am Main, Germany, with a subsidiary in the US. More at: www.schlafenderhase.com

November 9, 2021

Schlafender Hase Team

Francisco Baraona Appointed Co-CEO of Schlafender Hase

Schlafender Hase has announced that Francisco Baraona joins the company as its co-CEO, effective November 1, 2021. He shares responsibility for operations with Frank Hessler, founding CEO of Schlafender Hase.

SEE ALL Press Releases

Videos

The Never-Ending Leafleats

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

eBooks

Med Device E-labelling

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives. 

Barcode grading e-book

January 31, 2023

Schlafender Hase Team

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.

Benefits of tvt

January 13, 2023

Schlafender Hase Team

TVT Benefits Booklet

Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees’ stress and ensured patient safety with an efficient proofreading workflow. 

SEE ALL eBooks

Publications

Medical Device Labelling

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

life sciences industry

November 2, 2022

Schlafender Hase Team

Change Management

As they try to plug the gaps, and hang on to the qualified and experienced experts they already have, life sciences companies need to be clever about how they support those people to make best use of the time, and how they alleviate the aspects of their job which add the least value professionally yet cannot be skimped on.

Routine Recall Risks

February 17, 2021

Schlafender Hase Team

The Devil in the Detail: 5 Routine Recall Risks Faced by Modern Pharma

With the steely eyes of the regulators firmly trained on everything that life sciences organisations do, the last thing firms want is to incur fines, market delays or worse because of overlooked mistakes in labelling and product information. Yet incidences of labelling issues and associated product recalls are rising sharply, now accounting for over 50% of all recalls according to the FDA. The conditions are rife for the trend to continue, due to growing complexity in life sciences firms’ operations and external market requirements.

SEE ALL Publications

Webinars

Digitizing Your Proofreading Workflow 

Schlafender Hase Team

Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

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.

Webinar: Level up with TVT 11

Schlafender Hase Team

Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

Webinar: e-PIL legislation

Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit. 

SEE ALL webinars

Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

SEE ALL CASE STUDIES

Blogs

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 Ways You’re Wasting Time & Money in Regulatory Affairs

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we’ll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

SEE ALL BLOGS

Press Releases

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.

LexisNexis® Reed Tech™

April 26, 2022

Schlafender Hase Team

LexisNexis® Reed Tech™ and Schlafender Hase® Alliance Provides Mutual Customer Benefits for Pharmaceutical and Medical Device Companies

Founded in 2001, Schlafender Hase GmbH is headquartered in Frankfurt am Main, Germany, with a subsidiary in the US. More at: www.schlafenderhase.com

November 9, 2021

Schlafender Hase Team

Francisco Baraona Appointed Co-CEO of Schlafender Hase

Schlafender Hase has announced that Francisco Baraona joins the company as its co-CEO, effective November 1, 2021. He shares responsibility for operations with Frank Hessler, founding CEO of Schlafender Hase.

SEE ALL Press Releases

Videos

The Never-Ending Leafleats

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

eBooks

Med Device E-labelling

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives. 

Barcode grading e-book

January 31, 2023

Schlafender Hase Team

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.

Benefits of tvt

January 13, 2023

Schlafender Hase Team

TVT Benefits Booklet

Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees’ stress and ensured patient safety with an efficient proofreading workflow. 

SEE ALL eBooks

Publications

Medical Device Labelling

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

life sciences industry

November 2, 2022

Schlafender Hase Team

Change Management

As they try to plug the gaps, and hang on to the qualified and experienced experts they already have, life sciences companies need to be clever about how they support those people to make best use of the time, and how they alleviate the aspects of their job which add the least value professionally yet cannot be skimped on.

Routine Recall Risks

February 17, 2021

Schlafender Hase Team

The Devil in the Detail: 5 Routine Recall Risks Faced by Modern Pharma

With the steely eyes of the regulators firmly trained on everything that life sciences organisations do, the last thing firms want is to incur fines, market delays or worse because of overlooked mistakes in labelling and product information. Yet incidences of labelling issues and associated product recalls are rising sharply, now accounting for over 50% of all recalls according to the FDA. The conditions are rife for the trend to continue, due to growing complexity in life sciences firms’ operations and external market requirements.

SEE ALL Publications

Webinars

Digitizing Your Proofreading Workflow 

Schlafender Hase Team

Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

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.

Webinar: Level up with TVT 11

Schlafender Hase Team

Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

Webinar: e-PIL legislation

Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit. 

SEE ALL webinars

Press Releases

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.

LexisNexis® Reed Tech™

April 26, 2022

Schlafender Hase Team

LexisNexis® Reed Tech™ and Schlafender Hase® Alliance Provides Mutual Customer Benefits for Pharmaceutical and Medical Device Companies

Founded in 2001, Schlafender Hase GmbH is headquartered in Frankfurt am Main, Germany, with a subsidiary in the US. More at: www.schlafenderhase.com

November 9, 2021

Schlafender Hase Team

Francisco Baraona Appointed Co-CEO of Schlafender Hase

Schlafender Hase has announced that Francisco Baraona joins the company as its co-CEO, effective November 1, 2021. He shares responsibility for operations with Frank Hessler, founding CEO of Schlafender Hase.

SEE ALL Press Releases

Blogs

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 Ways You’re Wasting Time & Money in Regulatory Affairs

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we’ll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

SEE ALL BLOGS

Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

SEE ALL CASE STUDIES

Videos

The Never-Ending Leafleats

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

eBooks

Med Device E-labelling

January 31, 2023

Schlafender Hase Team

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives. 

Barcode grading e-book

January 31, 2023

Schlafender Hase Team

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.

Benefits of tvt

January 13, 2023

Schlafender Hase Team

TVT Benefits Booklet

Read the Benefits Booklet to learn how TVT has helped companies in Life Sciences decrease their employees’ stress and ensured patient safety with an efficient proofreading workflow. 

SEE ALL eBooks

Publications

Medical Device Labelling

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

life sciences industry

November 2, 2022

Schlafender Hase Team

Change Management

As they try to plug the gaps, and hang on to the qualified and experienced experts they already have, life sciences companies need to be clever about how they support those people to make best use of the time, and how they alleviate the aspects of their job which add the least value professionally yet cannot be skimped on.

Routine Recall Risks

February 17, 2021

Schlafender Hase Team

The Devil in the Detail: 5 Routine Recall Risks Faced by Modern Pharma

With the steely eyes of the regulators firmly trained on everything that life sciences organisations do, the last thing firms want is to incur fines, market delays or worse because of overlooked mistakes in labelling and product information. Yet incidences of labelling issues and associated product recalls are rising sharply, now accounting for over 50% of all recalls according to the FDA. The conditions are rife for the trend to continue, due to growing complexity in life sciences firms’ operations and external market requirements.

SEE ALL Publications

Webinars

Digitizing Your Proofreading Workflow 

Schlafender Hase Team

Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

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.

Webinar: Level up with TVT 11

Schlafender Hase Team

Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

Webinar: e-PIL legislation

Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit. 

SEE ALL webinars

Videos

The Never-Ending Leafleats

Top Pharma Automate Proofreading

TVT Barcode Video

SEE ALL Videos

Blogs

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

5 Ways You’re Wasting Time & Money in Regulatory Affairs

March 1, 2023

Schlafender Hase Team

5 Ways You’re Wasting Time & Money in Regulatory Affairs

If you are proofreading manually, you are aware of how time-consuming it is. We have all heard the saying “time is money”, and this is very true for Regulatory Affairs professionals. In this article, we’ll be exploring proofreading in Regulatory Affairs, and 5 ways that RA depts. are wasting money by relying on manual proofreading.

SEE ALL BLOGS

Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

SEE ALL CASE STUDIES

Press Releases

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.

LexisNexis® Reed Tech™

April 26, 2022

Schlafender Hase Team

LexisNexis® Reed Tech™ and Schlafender Hase® Alliance Provides Mutual Customer Benefits for Pharmaceutical and Medical Device Companies

Founded in 2001, Schlafender Hase GmbH is headquartered in Frankfurt am Main, Germany, with a subsidiary in the US. More at: www.schlafenderhase.com

November 9, 2021

Schlafender Hase Team

Francisco Baraona Appointed Co-CEO of Schlafender Hase

Schlafender Hase has announced that Francisco Baraona joins the company as its co-CEO, effective November 1, 2021. He shares responsibility for operations with Frank Hessler, founding CEO of Schlafender Hase.

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eBooks

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Blogs

Medical Device Labelling

March 16, 2023

Schlafender Hase Team

Digital Transformation of Medical Device Labelling: A Practical Guide

By allowing medical device suppliers to provide up-to-date, reliable product and safety information in a secure and accessible format, e-labelling has the potential to revolutionise how medical professionals and patients access and manage information. In this article, Peter Muller of Schlafender Hase examines the potential of e-labelling and recommends practical steps to secure the benefits of e-labelling.

What is a document comparison software?

March 15, 2023

Schlafender Hase Team

What is Document Comparison Software and Why You Need it if You Are in Regulatory Affairs?

The major players in the Pharma and Medical Devices industries have either adopted or are in the process of adopting a software for document comparison. Like other technologies, this too has been a slow adoption despite it’s proven time, money, and stress savings. The goal of this article is to explain how document comparison software can help and why it is an essential part of any Regulatory Affairs tech stack.

8_WAYS_TO_GET_YOUR_PRODUCT_TO_MARKET_FASTER

March 2, 2023

Schlafender Hase Team

8 Ways RA can help get Products to Market Faster

Bringing a new drug to market is time-consuming and costly, and generally takes 10 years and costs over $1 billion. The smallest lapse in labeling and packaging can jeopardize even the most well-planned submission. A proofreading and comparison software can help you get there faster, safer.

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Case Studies

January 26, 2023

Schlafender Hase Team

New World Medical – Saving Resources and Increased Efficiency for Proofreaders

With implementation of TVT in its quality assurance department, New World Medical is achieving significant time savings. It now also plans to roll out the automated proofreading solution from Schlafender Hase across other parts of the company.

National Regulatory Authority

September 29, 2022

Schlafender Hase Team

How a National Regulatory Authority Increased Their Proofreading Targets by Over 50%

‘’TVT has contributed to a 50% increase in targets, which is truly more than we expected from any electronic solution,’’ reiterates the senior manager in the unit. ‘’It has given our team the ability to streamline our proofreading process and focus on improving our internal procedures.’’

Mot. Tiff Case Study

August 23, 2022

Schlafender Hase Team

Mot. Tiff – Quality, Traceability and Right First Time with TVT, the Text Verification Tool

Since Mot.Tiff introduced TVT, the Text Verification Tool from Schlafender Hase, its clients have benefited from higher quality, faster text turnarounds, traceable audit trails and significant time savings in the pharmaceutical and fast moving consumer goods sectors.

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Press Releases