November 17, 2020
Schlafender Hase Team
If you would like to know more about TVT Connect and integration with information management systems, contact us:
If you would like to know more about TVT Connect and integration with information management systems, contact us:
October 8, 2020
Schlafender Hase Team
Yes, this can be a common situation: a Brand Owner submits the packaging or labeling brief in multiple file formats using an Excel spreadsheet combined with a Word document. Critical, legally required table information such as nutrition facts and allergens arrive in Excel templates. These Excel files are used to generate label revisions which comply with FDA regulations.
Yes, this can be a common situation: a Brand Owner submits the packaging or labeling brief in multiple file formats using an Excel spreadsheet combined with a Word document. Critical, legally required table information such as nutrition facts and allergens arrive in Excel templates. These Excel files are used to generate label revisions which comply with FDA regulations.
October 1, 2019
Schlafender Hase Team
Schlafender Hase’s proofreading software, TVT®, the Text Verification Tool®, has been catching errors on packaging and labels of life sciences products for 15 years now. CEO Frank Hessler and Head of Marketing, Kindrie Eaton take a look at the company’s past with a view toward its future and their rebrand.
Schlafender Hase’s proofreading software, TVT®, the Text Verification Tool®, has been catching errors on packaging and labels of life sciences products for 15 years now. CEO Frank Hessler and Head of Marketing, Kindrie Eaton take a look at the company’s past with a view toward its future and their rebrand.
July 25, 2019
Schlafender Hase Team
The regulation on medical devices 2017/745, widely known as the EU MDR, was released in May 2017 with regulation 2017/746 on in vitro diagnostics. EU MDR and regulation 2017/746 replaced Council Directive 93/42/EEC, also known as the Medical Device Directive (MDD), and Directive 98/79/EC on in vitro diagnostic medical devices.
The regulation on medical devices 2017/745, widely known as the EU MDR, was released in May 2017 with regulation 2017/746 on in vitro diagnostics. EU MDR and regulation 2017/746 replaced Council Directive 93/42/EEC, also known as the Medical Device Directive (MDD), and Directive 98/79/EC on in vitro diagnostic medical devices.
June 13, 2018
Schlafender Hase Team
The majority of medical device recalls are due to labeling or software - HMI issues. TVT can help keep you from becoming a statistic.
The majority of medical device recalls are due to labeling or software - HMI issues. TVT can help keep you from becoming a statistic.
August 17, 2015
Schlafender Hase Team
Below are what I consider as the top 2 biggest misunderstandings regarding electronic proofreading.
Below are what I consider as the top 2 biggest misunderstandings regarding electronic proofreading.
