As technology advances, more and more opportunities arise in medical technology. Components are becoming increasingly smaller and more powerful, and the Internet of Things and the cloud offer completely new potential. However, special guidelines apply in particular in the medical field, for example for working in clean room environments and for testing new medicines and devices on living beings.
We support you in setting up quality management systems according to ISO 13485, FDA and MDR. In addition, we create documents and specifications for production in clean room class 8. We also carry out internal audits and process audits for you and carry out root cause analyzes and risk assessments. For further services, please have a look at our portfolio pages or contact us directly.