We are pleased to present you our brand new whitepaper! Thanks to the collaboration between Europe IT Consulting GmbH and Opal Labelmanagement, we have created this comprehensive guide that provides you with in-depth knowledge and practical guidance on how to design compliant labels according to the EU MDR 2017/745 Regulation.
In our whitepaper, you will get valuable tips and recommendations on the regulatory and complex environment of Unique Device Identification (UDI). We mention topics such as EU legislation, the new ISO standard 20417:2021 as well as the various requirements of the printing process.
Highlights of the white paper include:
- A comprehensive checklist for MDR-compliant labels.
- Explanations of the specific requirements for data management and transfer to EUDAMED.
- A detailed sample label that addresses all requirements and can be ordered as a reference poster.
Don’t miss this chance to update your knowledge and ensure your products meet the latest EU standards.
Related Posts