Working Effectively with Notified Bodies

When releasing medical devices in the European market, manufacturers face many complex rules to ensure compliance with the EU’s health, safety and environmental regulations. Notified… Read More

Understanding EUDAMED: Its Role in EU Medical Device Regulation

EUDAMED, the European Database on Medical Devices, is a central part of the EU’s medical device regulatory landscape. This centralized hub houses critical information about… Read More

Stop the Clock: Revised IVDR Deadlines Offer MDMs a Timely Advantage

Manufacturers of in vitro medical devices who may be anxious over looming deadlines posed by Europe’s regulations have been given some breathing room. In January… Read More

Understanding the EU MDR and Post-Brexit Regulatory Changes

As we move into 2024, the Life Sciences sector in Europe and the UK continues to face a dynamic and challenging regulatory environment. The… Read More

Argos Multilingual Releases Upgraded AI Translation Memory Cleanup Service

San Francisco (CA), January 17, 2024 – Argos Multilingual, a leader in the global content solutions market, has announced the release of a significantly upgraded… Read More

6 Ways a Centralized Translation Model Can Support Your MDR and IVDR Compliance 

As the life sciences industry continues working to comply with the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Devices… Read More

How to use DTP with Translation to Maximize Impact in Every Market

Whether you are conscious of it or not, design has a tremendous effect on our daily life: What captures our attention, how long an… Read More

Use This Time Wisely: Seven Proactive Steps to Take Now for EU MDR and IVDR Compliance

Medical device manufacturers (MDMs) have various resources to ensure compliance with the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Recently, the… Read More

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