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Tag: medical device

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

Event

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22 Jun 2020

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...

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