Ultimate guide to placing a medical device on the EU market

Every medical device start-up dreams of market success and that first influx of revenue. But until you secure EU approval, the vast European market of half-a-billion people remains barred shut - and your company continues to spend money with nothing in return.

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What you'll learn

Understand the end-to-end process for launching a medical device in the EU, and how long it will take

Unpick the key steps to market, from classifying your device and building a QMS to passing your conformity assessments and audits

Understand the right timing for creating your quality documents and applying for CE marking

Hear tips and best practice for a faster, more targeted route to market

Speakers

Sumatha Kondabolu

Tanja Rohark