Breakfast and Learn | Software regulation as a Medical Device 

September 9, 2022

📆 September 14    🕘 9:00 a.m.

Join Asphalion expert Talyta Carteano, Medical Device Associate Director & Lead Auditor in this talk, where she will help identifying medical devices and go through their regulation, an important aspect for research teams to take into account when starting projects that involve these technologies.

Furthermore, she will talk about the creation processes of MD, the steps to follow in order to carry out clinical trials and research, as well as the main aspects in order to commercialize these technologies.

There will be time to answer Q&As from the audience at the end of the session.

The session will be held in Spanish.

Registration is free and is open:

Check here for further information:

Search News & Events

  • Filter by category


Related news and events


Achieving CE Marking is crucial for medical devices intended for the European market. Asphalion MedTech, a specialized unit within Asphalion, provides comprehensive guidance and expert

For further information

If you are interested in our services, or wish to get in touch for a general enquiry, please contact us for more information.

Fill the form and we will contact you as soon as possible.

You can also follow us on:

Schedule a Free Meeting

Schedule here a free 30-minutes meeting with one of our consultants and tell us about your project, challenges or doubts. 

We will be happy to assist you!

Schedule a meeting