DO YOU KNOW HOW TO MAKE THE MOST OF YOUR CAPA PROCESS?

Events

Within the healthtech industry, corrective and preventive actions, also known as CAPA, is one of the most critical quality management system processes, enhancing the manufacturers’ overall commitment to continuously improve their quality management systems.

Now is your chance to learn more about CAPA! On Wednesday 12 February, our expert on medical devices Merja Vainio will give a lecture on CAPA at the European Medical Device and Diagnostic Quality Management Conference in Brussels.

In addition to gaining a thorough understanding of the basics, definitions and requirements of CAPA, the attendees will learn how to implement and develop an efficient and effective CAPA process.

If you are attending the conference and have any questions related to CAPA, QMS or medical devices, please don’t hesitate to book a meeting or simply have a chat with Merja.

Can’t attend the conference? No problem, you can contact us by sending an email to contactus@medfiles.eu or by contacting our Regulatory Affairs Manager Päivi Turta.

Päivi Turta Medfiles
Päivi Turta
Regulatory Affairs Manager
paivi.turta@medfiles.eu

+358 50 313 0323

The Medfiles Medical Device Team is always happy to help you!

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