MENU menu

IVDR Celebration Week Session 3


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 3 – Wednesday 27th April 2022 @ 11:00 AM BST - IVD Medical Device - Understanding SaMD and Cyber Security Requirements


The thriving MedTech industry has several regulatory requirements. Even medical 'software', A.I. components and Machine Learning algorithms have 'hard' regulatory requirements but why should regulation hold back your innovation?


Our experts from Med-Di-Dia and Global Regulatory Services are here to help you better understand the Internet of Medical Things (IoMT), SaMD and cyber security along with the regulatory requirements which must be adhered to.


Tune in to interact with Greer Deal – Director and Paul Butcher – Cyber Security Expert from GRS and our very own David Didsbury -  ALaMD Expert on Wednesday 27th April 2022 at 11:00 AM BST


Have any specific questions?

Need direct answers?

Drop them to and our experts will be happy to help.

Don't Let Regulations Hold Back your Innovation.


IVD Medical Device - Understanding SaMD and Cyber Security Requirements

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 


IVDR Cyber security and SaMDIVDR Ready





Get access to the Med-Di-Dia’s newsletter, where industry experts help you to stay on top of shifting global markets.

Stay updated with the latest Trends in the world of Medical Devices!


* indicates required