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Medical Device Manufacturer

July 25, 2019

Schlafender Hase Team

Are You a Medical Device Manufacturer?

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.

Medical Device Manufacturer
4 minutes read

Are You a Medical Device Manufacturer?

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.

Medical Device Recalls

June 13, 2018

Schlafender Hase Team

Medical Device Recalls

The majority of medical device recalls are due to labeling or software - HMI issues. TVT can help keep you from becoming a statistic.

Medical Device Recalls
< 1 minute read

Medical Device Recalls

The majority of medical device recalls are due to labeling or software - HMI issues. TVT can help keep you from becoming a statistic.

Electronic Proofreading

August 17, 2015

Schlafender Hase Team

2 Biggest Myths in Electronic Proofreading

Below are what I consider as the top 2 biggest misunderstandings regarding electronic proofreading.

Electronic Proofreading
< 1 minute read

2 Biggest Myths in Electronic Proofreading

Below are what I consider as the top 2 biggest misunderstandings regarding electronic proofreading.