Is your company ready for the digital future and compliance with In Vitro Diagnostic Regulation (IVDR 2022) and EU MDR (2024)? Practical know-how; digital tools and processes needed
The European Parliament has set forth new regulatory requirements for post-market surveillance (PMS). The current In Vitro Diagnostic Directive (IVDD) will be replaced with the In Vitro Diagnostic Regulation (IVDR) which will fully apply...
