Labelling Compliance for Medical Devices: Wanted Global Harmonisation!
Add bookmark
Labelling Compliance for Medical Devices: Wanted Global Harmonisation!
Add bookmark
Peter Schroeer, Director Europe, Quality Systems & Regulatory Affairs at Johnson & Johnson, speaks to Andrea Charles from Pharma IQ, about the current compliance challenges the medical device market faces and what impact the reuse warning statement requirement per directive 2007/47/EC has had on global labeling strategies. He also shares his top 3 tips for defining and implementing a global labeling strategy and his insights on what future global developments we will see in regulatory compliance.
[inlinead]
Tags:
Peter Schroeer
medical device packaging
medical device labelling compliance
medical device market
single use medical devices
reuse of single use medical devices
directive 2007/47/EC
global labeling strategies
regulatory compliance
