IVDR Celebration Week Session 4

Med-Di-Dia and Global Regulatory Services are organising a series of weeklong fireside chats to celebrate the incoming IVD Regulations in the European Union.

This is a big buzz in the MedTech and regulatory space. For the first time, In-Vitro Diagnostic Medical Devices are coming under a strict regime and vigilance dedicated to this sector. IVDR (In-Vitro Diagnostic Regulations) will be succeeding the MDD (Medical Device Directives) and will be enforceable from 26^th May 2022

Session 4 – Wednesday 27^th April 2022 @ 2:00 PM BST - IVD Medical Device - the need for UDI and Barcodes

EUDAMED, UDI, Harmonisation, sounds like a lot?

Wondering what this all means? Join us on Wednesday 27^th April @ 2:00 PM BST, where Greer Deal – Director - Global Regulatory Services (GRS), declutters the nuances around Harmonization and Standardization. Want to implement the correct UDI Practices? Our Resource Partner – Amanda Creane – Healthcare Manager - GS1 Ireland, shall enlighten us all with the magic of GS1 standards for UDI and other barcoding practices.

Have questions around this topic?

Send us an email: mdd@mddltd.com

We are your regulatory risk partners for Medical Devices, Diagnostics and Digital Health!

IVDR Celebration Week - IVD Medical Device - the need for UDI and Barcodes