Why IVDR coding?
The In Vitro Diagnostic Medical Device Regulation (IVDR) coding system indicates conformity assessment activities and device types a Notified Body (NB) is authorized to assess following designation.
In our latest white paper, "Coding under the IVDR", we explore the codes, their importance and how we can help.
What you'll find in our white paper
- Defining the Commission Implementing Regulation (EU) 2017/2185A brief look at the companion regulation and its goals.
- The codes laid bareFrom IVR and IVS to IVT, IVP and IVD, we explore each in detail.
- Code coverageWe outline each code’s area, including blood grouping, tissue typing and cancer markers.
- SGS as an IVDR Notified BodyAs a designated IVDR NB, we outline our capabilities and how we are ready to help.