How to comply with the MDR requirements for medical device labels
Kristina Zvonar Brkic
According to the definitions in the European Union’s Medical Device Regulation (MDR) (Article 2), “label” means any written, printed, or...
According to the definitions in the European Union’s Medical Device Regulation (MDR) (Article 2), “label” means any written, printed, or graphic information appearing either on the device itself, or on the packaging of each unit...
