XTM Live is right around the corner. We are looking forward to sponsoring the event! Drop by to say hello at booth #2 if you will be attending, or reach out to Antoine Rey and Rodrigo Cristina, and they would be happy to set up a time to chat at the event. eu1.hubs.ly/H03rC_D0

We have a big announcement today. Alexander Ulichnowski has taken on the role of CEO at Argos! We are excited for this next chapter as a company. eu1.hubs.ly/H06Fdhn0

Medical translations where precision is paramount. 🩺 Partner with Argos Multilingual, a trusted name for life sciences and medical translations. Explore more: 🔗eu1.hubs.ly/H06Fq1S0 #LifeSciencesTranslation #MedicalDevices #LifeSciences

Navigate the complexities of EU MDR with ease. 🌍 From timelines to critical FAQs, we provide all the information you need about MDR in one place. 🔗 eu1.hubs.ly/H06FpZw0 #EUMDR #medicaldeviceregulation #medicaldevices #MDRCompliance

🚀 New Release: Uncover the essentials of #EUMDR with Argos Multilingual's eBook. Stay updated, stay compliant. Download now. 📚 🔗 eu1.hubs.ly/H06LWHf0 #EUMDR #medicaldeviceregulation #medicaldevices #MDRCompliance

Preparing for EU MDR & IVDR? Translation is key. Our checklist will help you make sure nothing is overlooked. Discover more: 👇 🔗eu1.hubs.ly/H06LWsP0 #EUMDR #medicaldeviceregulation #medicaldevices #MDRCompliance

Medical device professionals: Explore the EU Medical Device Regulation with our comprehensive eBook. Understand ISO standards, the nuances of CE marking and translation requirements to remain informed in a shifting regulatory environment. 🔗 eu1.hubs.ly/H06HRC20 #EUMDR

Dive into the details of #EUMDR with Argos Multilingual's eBook and understand: ✅ When to provide electronic instructions for devices. ✅ The translation requirements for MDR. ✅ Restrictions on symbol usage. 🔗 eu1.hubs.ly/H06HRJ10 #medicaldeviceregulation #MDRCompliance

The EU Medical Device Regulation (MDR) consolidated 28 regulations into one and made the role of translation crucial. Argos Multilingual's guide covers ISO 13485:2016 for LSPs & EU language requirements. Ensure compliance & stay ahead: 🔗 eu1.hubs.ly/H06HRPN0 #EUMDR

Navigating the EU Medical Device Regulation (MDR) for Instructions for Use (IFUs)? Argos Multilingual's guide breaks down MDR requirements, from IFU essentials to EU language specifications. Discover more: 🔗 eu1.hubs.ly/H06HRCw0 #EUMDR #medicaldeviceregulation

📘 Navigating the EU's #IVDR? Our eBook has you covered. Discover new classifications and why UDI is crucial. Ensure content & translation compliance with Argos Multilingual. 🔗 eu1.hubs.ly/H06HRGY0 #IVDR #InVitroDiagnosticRegulation #medicaldevices #IVDRCompliance

📘 Ready to tackle MDR & IVDR compliance head-on? Our guide offers a roadmap for success. Navigate reclassification, enhance labeling, and meet EU market standards. 🔗 eu1.hubs.ly/H06HRP60 #EUMDR #IVDR #InVitroDiagnosticRegulation #medicaldevices #IVDRCompliance

📘 Understand the #EUMDR with Argos Multilingual's eBook. Dive into translation requirements, the role of notified bodies, and device documentation in the EU market. Stay informed, agile, and ready to respond to the latest changes in regulations. 🔗 eu1.hubs.ly/H06HRCp0

📘 Explore the world of a centralized Life Sciences content strategy. Our eBook looks at key pillars, from unified language to adaptability. Get your copy now. 🔗 eu1.hubs.ly/H06HRQ40 #lifesciences #contentstrategy #centralizedcontent

🏥 EU Medical Device Regulations are reshaping the industry. Our eBook explores the impact on translation requirements, UDI, quality, and more. Stay compliant and informed. 🔗 eu1.hubs.ly/H06HRLM0 #medicaldeviceregulation #medicaldevices #MDRCompliance

The EU IVDR has reshaped how in vitro medical devices are marketed and sold in Europe. 🌍 Gain insights on its major changes, new classifications, and its impact on content and translation strategies with our comprehensive guide. 🔗 eu1.hubs.ly/H06HRHY0 #IVDR #IVDRCompliance