CE Marking Conformity Assessment for Medical Devices

Download our white paper on CE Marking Conformity Assessment Options in the EU

In this white paper, learn to how to identify the best conformity assessment route for your device under the MDD.

Questions? Request more information from our specialists


Ready to sell your medical devices in Europe? First, you must comply with Europe’s medical device regulations. But instead of a one-size-fits-all approach, there are many ways to demonstrate your compliance – also known as conformity assessment routes.

The conformity assessment route makes it easy for the Notified Body to verify your compliance to the MDD and Essential Requirements. There are many routes to choose from, and your chosen route has implications for your business that you might not expect. How do you know which route is best for you?

What you will learn in this 4-page white paper:

  • How does device classification dictate the conformity assessment route?
  • Are some routes more cost effective?
  • What is the fastest route to achieve CE Marking?
  • What factors should I consider when choosing a conformity assessment route?
  • How does my chosen route affect my business?

We answer all of these questions and many more in this whitepaper.