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18 August 2023

Streamlining Medical Device Design and Development Under EU MDR 2017/745: A Comprehensive Guide

In a world where healthcare is evolving at an unprecedented pace, the design and development of medical devices demand meticulous attention to detail. The European Union’s […]
4 July 2022

Documentation control in ISO 13485

Moving to an e-QMS (electronic QMS) solution shall help you with the documentation control, since many of the steps would be automatized and you would need […]
14 June 2022

Advantages and disadvantages of e-QMS in medical device companies

The use of online solutions for the compliance with voluntary standards and legal regulations are becoming more popular among any size of companies of every sector […]
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