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Gokhan Toros 4 min. read
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 EU extended these deadlines, giving manufacturers more time for compliance. For instance, conformity assessments for higher-risk devices (class IIb and class III) are now due in 2027, while lower-risk devices […]

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Use This Time Wisely: Seven Proactive Steps to Take Now for EU MDR and IVDR Compliance
mgorczyca 13 min. read
Building and Growing Language Operations in Life Sciences

In an increasingly globalized healthcare landscape, the importance of accurate and effective language translation cannot be overstated, particularly in the life sciences sector. With this focus, Argos Multilingual recently convened a distinguished panel of experts for a webinar entitled “Building and Growing Language Operations in Life Sciences.“ The panel delved into the intricacies and challenges […]

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Building and Growing Language Operations in Life Sciences
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