Do you need to be certified to operate in the medical device market?

ISO13485 certification

In partnership with Le Village By CA, Cisteo offers you a Live on the theme of ISO 13485: 2016 certification. Lauriane Sauge, head of quality and regulatory services at Cisteo, will address the challenges and benefits of entering into an ISO 13485 certification process.

Why and how to obtain ISO 13485 certification?

You are a subcontractor, manufacturer or any new player in the medical devices market and you have questions about ISO 13485 certification. This webinar is an opportunity to address these questions and provide you with concrete answers tailored to your needs.

The themes covered around ISO 13485 certification

In order to provide you with a global vision, we will cover the following topics in particular:

  • Normative and regulatory context
  • Is it mandatory to be ISO 13485 certified?
  • Why be certified?
  • Fears: between cost and administrative burden, how can we see things more clearly?
  • How to access certification?

Watch the replay

If you missed the webinar or would like to watch it again, find the replay below:

Other articles to explore

Right from the design phase, Cisteo MEDICAL puts mechatronics to work for AIMDs

Cisteo MEDICAL aims to push back the limits of embedded systems, such as size and autonomy. The company supports its customers...
Read more
Active implantable medical device pacemaker

Cisteo MEDICAL extends its ISO 13485 certification to active implants and software

We are pleased to announce the renewal of our NF EN ISO 13485: 2016 certification. A good...
Read more
contract manufaction organisation presentation

A new brochure to present our contract manufacturing activities

Find a summary of our activities in our new brochure. As a global partner of medical device manufacturers,...
Read more

To find out more, book an appointment with one of our specialists and let's talk about your projects!

Plus buttonContact us
Decoration block gray
More Information