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

ISO13485 certification, standard for medical devices

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

Alison ++, an AI-powered medical device

Alison++: The consortium that puts AI at the service of resuscitation

In intensive care, nursing teams face a constant challenge: maintaining their patients in a state of sedation...
Read more
Nitinol stent

Article DeviceMed: Recent advances in nitinol stent design

In parallel with its active implant activities, Cisteo MEDICAL designs, under contract, medical devices in nitinol and a...
Read more
Diag Medical devices from BPI France

Diag DM, a subsidy for medical device manufacturers

Available in class IIa and above, Diag DM is a device that allows you to benefit from a comprehensive...
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