25 May 2023

How to make labelling regulatory compliant for EU-MDR (2017/745)

The European Union Medical Device Regulation (EU MDR), effective from 2028, aims to enhance the safety and effectiveness of medical devices sold within the European Union. Compliance with the EU MDR is crucial for manufacturers to meet regulatory standards and ensure optimal patient outcomes. 

One key aspect of compliance is labelling remediation, which involves reviewing and updating existing labelling to adhere to the new regulations

UI/UXDesign webinar

Overall, UI/UX is crucial as it directly impacts customer perception, influencing their decision to engage, purchase, and advocate for a product or service. Choosing the right UX method depends on the specific goals and constraints of your project & various factors, including user needs, and available resources. 

Please watch the full webinar to learn more about UI/UX design. 

This webinar was presented by Decos, a cutting-edge technology services partner ready to meet your diversified needs in the healthcare domain.

If you have any questions about this webinar or wish to seek advice on UI/UX design, please contact Devesh at devesh.agarwal@decos.com

We would love to discuss it with you! 


Discover more

Materials behaviour
The Ethics of Material Behaviour
In today's world, where material science innovation is constantly pushing boundaries, the ethical implications of our material choices often go overlooked. This technical webinar delves...
Read more
health tech
Cloud Computing Trends in Healthcare: IoMT, AI, and Blockchain Integration
"Cloud Computing Trends in Healthcare: IoMT, AI, and Blockchain Integration" webinar presented an in-depth exploration of cutting-edge technologies revolutionizing the healthcare sector.
Read more
Use related hazards
Identifying, prioritizing, and controlling use-related risks in medical devices
Medical device use error refers to any mistake or failure in the use of a medical device that could lead to harm to the patient...
Read more