TVT Resources | Schlafender Hase

October 27, 2021

Schlafender Hase Team

Webinar: Make Sure Your Barcode Makes the Grade

In this webinar you will learn how TVT Barcode identifies barcode errors before they are printed and automatically detects, decodes, compares and grades barcodes used by highly regulated industries like Life Science.

2 minutes read

Webinar: Make Sure Your Barcode Makes the Grade

October 26, 2021

Schlafender Hase Team

Schlafender Hase® Releases TVT Barcode

TVT Barcode is an add-on module that has been released with the new TVT® version 10.2. It has been designed for use across all industries, including the highly regulated pharmaceutical and medical devices industries.

2 minutes read

Schlafender Hase® Releases TVT Barcode

October 20, 2021

Schlafender Hase Team

Live vs. Rasterized vs. Vectorized Text

In a previous post, we covered the basics of Unicode and why it’s so important for proofreaders (or anyone involved in the document creation, review and correction workflow) to understand the differences between the way humans and computers read language. Today, we’ll build on that knowledge as we examine different ways design and print proofs can be exported to PDF and the risks associated with removing live text from your organization’s documents.

4 minutes read

Live vs. Rasterized vs. Vectorized Text

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.

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.

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.

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.

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.

2 minutes read

MDR Graphic Symbols

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

September 30, 2021

Schlafender Hase Team

Medical Devices Regulation EU 2017/745

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

2 minutes read

Medical Devices Regulation EU 2017/745

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

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,

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,

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.

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.