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IVDR Celebration Week Session 6


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 26th May 2022. 


Session 6 - Thursday 28th April 2022 @ 02:00 PM BST - Where to Start in order to launch an IVD Medical Device onto the EU Market


From idea to product commercialization – know about the importance of a Regulatory Strategy and how this will serve as the ultimate champion for launching your IVD medical device into Europe and beyond.

Learn LIVE from Greer Deal – Director – Global Regulatory Services (GRS) - the starting point for the successful commercialization of an IVD medical device. Also on hand is our Resource Partner, Steven Griffin – Health Innovation Hub Ireland (HIHI) – who will highlight the common aspects of the innovation process, how to overcome the pitfalls and what HIHI can offer to support the development process.


Catch us LIVE on Thursday 28th April 2022 @ 02:00 PM BST

Our experts are Driving Innovation to Market Success!

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Where to Start in order to launch an IVD Medical Device onto the EU Market

Link to Broadcasts 






Resource Partners 

Health Innovation Hub Ireland 

Medilink Midlands

Xenon Health Solutions 

Galway Chamber 

GS1 Ireland 

Afortiori Development

Embassy of India - Dublin, Ireland 


Launching medical device in EUHealth Innovation Hub Ireland Medical Device Regulatory Strategy Regulatory Strategy support for IVDR





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