Product Certification
The issue of product safety is now a priority for every manufacturer, as is the importance of knowledge of legislation and regulations to ensure the ultimate goal of 'preventive protection' for the consumer.
Thanks to Kiwa's expertise, medical device companies can demonstrate that they meet the essential requirements for medical devices and gain access to the European market, as well as obtaining prerequisites for access to other global markets. In addition, thanks to Kiwa Italia's technical expertise, medical device manufacturers can rely on a trusted partner that can guarantee the execution of an effective conformity assessment process, which can combine a guarantee of market protection with a business tool.
Our services in the field of product certification
- Medical Devices
- Product Certification
- Quality Management System Certification
- Laboratory Services
- Training Courses
- How do I get my medical device certified?
- Notified Bodies for medical devices
- Technologies and devices Kiwa can certify
- EU information and factsheet for manufacturers
- Why choose Kiwa for your CE marking approval?
The new regulations on medical devices
Read more about the regulatory framework on the EU website
Technologies and devices Kiwa can certify
Kiwa boast a wide and in-depth experience as Notified Bodies in medical devices certification, with thousands of products already certified.