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.

Got questions? Don’t hesitate to Contact Us to find out more about our life sciences translation services.

Want to know more?

• Webcast: E-Labeling for Medical Device Manufacturers – Part 1
• Whitepaper: The New EU Medical Device Regulations