February 21, 2022
Schlafender Hase Team
Ready to put an end to repetitive correction cycles?
Ready to put an end to repetitive correction cycles?
January 4, 2022
Schlafender Hase Team
Pharma 4.0 is changing the landscape of the pharmaceutical industry, with a similar quiet revolution also taking place in proofreading through automation and transparency. This is illustrated by the enhancements in the new Version 10.2 of TVT®.
Pharma 4.0 is changing the landscape of the pharmaceutical industry, with a similar quiet revolution also taking place in proofreading through automation and transparency. This is illustrated by the enhancements in the new Version 10.2 of TVT®.
December 21, 2021
Schlafender Hase Team
Over the years, as we’ve worked to help make proofreading easier and more accurate for our customers, we’ve witnessed many different types of potential issues with labeling artwork design proofs. Most of these issues are visible to the human eye when reading through the document, but a few of them are invisible and require special techniques.
Over the years, as we’ve worked to help make proofreading easier and more accurate for our customers, we’ve witnessed many different types of potential issues with labeling artwork design proofs. Most of these issues are visible to the human eye when reading through the document, but a few of them are invisible and require special techniques.
November 17, 2021
Schlafender Hase Team
Unicode is a computer and software industry standard for handling text. While it is possible to geek-out on the technical aspects of Unicode (and if you’re so inclined you can check out the Wikipedia page on Unicode and the Unicode Consortium website), in this article we’re going to focus more on understanding the fundamentals, and discuss why this basic knowledge is critical for anyone who is part of a document creation / editing / review / correction workflow in a highly regulated industry.
Unicode is a computer and software industry standard for handling text. While it is possible to geek-out on the technical aspects of Unicode (and if you’re so inclined you can check out the Wikipedia page on Unicode and the Unicode Consortium website), in this article we’re going to focus more on understanding the fundamentals, and discuss why this basic knowledge is critical for anyone who is part of a document creation / editing / review / correction workflow in a highly regulated industry.
November 12, 2021
Schlafender Hase Team
Curious about the history of pharmaceutical recalls and the billions of dollars lost? Please see below for 10 pricey issues and the health risks associated behind the reason for the recalls.
Curious about the history of pharmaceutical recalls and the billions of dollars lost? Please see below for 10 pricey issues and the health risks associated behind the reason for the recalls.
October 20, 2021
Schlafender Hase Team
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.
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.
October 12, 2021
Schlafender Hase Team
Explore the impact of labeling errors on pharmaceutical recalls. Find out how to avoid these mistakes and maintain compliance with industry regulations.
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
The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.
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
Over the last few posts, we have been touching upon different labelling requirements set by the MDR.
Over the last few posts, we have been touching upon different labelling requirements set by the MDR.
