Thank you for visiting our site.
I imagine, you are involved in a medical device project. And your are in:
- The Research and Development phase
- The Regulatory or Clinical phase
- Setting up the production phase
- Preparation of Market Access phase
If you are earlier or later, you probably do not need our help
Unless of course you need a trained internal auditor (MDR 2017/745 & ISO 13485:2016)