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Take Your Medical Devices Global

Get in touch and tell us about your translation needs

Argo simplifies your global translation efforts through:

  • ISO 13485 Registration
  • International Regulation Procedures
  • Regulatory Compliance Platform Reporting
  • Full Project Audit Trail
  • Project Certification
  • Subject Matter Expert Translators

Trusted by Top Worldwide Brands

cardiac science logo medical devices
brany logo medical devices
preventis logo medical devices
orasure technologies logo medical devices

How Can Argo Make a Difference in Your Business? 

Translation for medical devices can be a complex process. Argo can help you bring your device to market by complying to your standard operating procedures as well as regulations set forth by the FDA, EU Medical Device Directives (MDD, AIMDD and IVDD) and other national and regional directives. Argo carries ISO 9001, 17100 and 13485 certifications in order to help you comply with your regulatory initiatives.  

Argo’s Regulatory Compliance Platform (RCP) provides secure online access and reporting capabilities to support your translation and localization procedures from start to finish. The system provides valuable information on all of the contributors to your projects for a complete audit trail of every task. The reports clearly list credentials and qualifications for all translators involved with your translation process. This set of procedures is key for any medical device manufacturer.

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