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Common Labeling Errors

October 12, 2021

Schlafender Hase Team

Common Labeling Errors That Lead to Pharmaceutical Recalls

Explore the impact of labeling errors on pharmaceutical recalls. Find out how to avoid these mistakes and maintain compliance with industry regulations.

Common Labeling Errors
4 minutes read

Common Labeling Errors That Lead to Pharmaceutical Recalls

Explore the impact of labeling errors on pharmaceutical recalls. Find out how to avoid these mistakes and maintain compliance with industry regulations.

MDR e-Labeling

October 6, 2021

Schlafender Hase Team

MDR e-Labeling

The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.

MDR e-Labeling
2 minutes read

MDR e-Labeling

The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.

MDR Graphic Symbols

October 6, 2021

Schlafender Hase Team

MDR Graphic Symbols

Over the last few posts, we have been touching upon different labelling requirements set by the MDR.

MDR Graphic Symbols
2 minutes read

MDR Graphic Symbols

Over the last few posts, we have been touching upon different labelling requirements set by the MDR.

Medical Devices Regulation

September 30, 2021

Schlafender Hase Team

Medical Devices Regulation EU 2017/745

Medical Devices Regulation (MDR) updates represent a step towards higher labeling standards.

Medical Devices Regulation
2 minutes read

Medical Devices Regulation EU 2017/745

Medical Devices Regulation (MDR) updates represent a step towards higher labeling standards.

MDR UDI and Device Registration

September 22, 2021

Schlafender Hase Team

MDR UDI and Device Registration

The new European Database on Medical Devices, known as EUDAMED, was originally scheduled to launch in May 2020,

MDR UDI and Device Registration
2 minutes read

MDR UDI and Device Registration

The new European Database on Medical Devices, known as EUDAMED, was originally scheduled to launch in May 2020,

TVT eLearning

September 6, 2021

Schlafender Hase Team

Top 3 reasons to encourage your employees to participate in e-Learning

As part of our TVT e-Learning portal we are offering a free trial to anyone interested in getting a feel for the system.

TVT eLearning
3 minutes read

Top 3 reasons to encourage your employees to participate in e-Learning

As part of our TVT e-Learning portal we are offering a free trial to anyone interested in getting a feel for the system.

PDF Artwork

August 25, 2021

Schlafender Hase Team

Top 8 Causes of PDF Artwork Mistakes: How to Avoid Errors in Labeling and Design

As you can see, the way in which the graphic designer / typesetter works as well as the tools and processes they use will influence the quality and content of the PDF Artwork.

PDF Artwork
3 minutes read

Top 8 Causes of PDF Artwork Mistakes: How to Avoid Errors in Labeling and Design

As you can see, the way in which the graphic designer / typesetter works as well as the tools and processes they use will influence the quality and content of the PDF Artwork.

Barcode Grading

August 11, 2021

Schlafender Hase Team

Make Sure Your Barcode Makes the Grade

In this interview, Mike Baird talks about TVT Barcode and what TVT customers can expect from this new module and the newly released version 10.2 of TVT, the Text Verification Tool.

Barcode Grading
4 minutes read

Make Sure Your Barcode Makes the Grade

In this interview, Mike Baird talks about TVT Barcode and what TVT customers can expect from this new module and the newly released version 10.2 of TVT, the Text Verification Tool.

Proofreading braille

July 15, 2021

Schlafender Hase Team

Four Tips for Regulatory Affairs to Proofread Braille

If you are part of a Labelling, Packaging, Graphics or Regulatory Affairs Department, these four tips will save time, and reduce risk and stress due to a missed error – even if you don’t have access to software capable of reading Braille. Since some European regulatory bodies mandate important information such as product name and dosage be written in Braille on packaging, knowing how to ensure Braille accuracy will be an asset for you and your specific life sciences company.

Proofreading braille
3 minutes read

Four Tips for Regulatory Affairs to Proofread Braille

If you are part of a Labelling, Packaging, Graphics or Regulatory Affairs Department, these four tips will save time, and reduce risk and stress due to a missed error – even if you don’t have access to software capable of reading Braille. Since some European regulatory bodies mandate important information such as product name and dosage be written in Braille on packaging, knowing how to ensure Braille accuracy will be an asset for you and your specific life sciences company.