Prepare Your Medical Devices for E-labeling
Find out why medical device manufacturers should consider moving toward e-labeling.
In this last of two Argos Multilingual webcasts about e-Labeling, we’ll begin by looking at the requirements which the European Commission has laid out in the regulation. We’ll look at why medical device manufacturers ought to consider acting sooner rather than later while offering some step-by-step pointers towards the end about how you should go about doing that.
Want to know more?
- Whitepaper: The New EU Medical Device Regulations