Medical Devices

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 9001:2015 and ISO 17100:2015 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 on every project. The reports clearly list credentials and qualifications for all translators involved with your projects. This set of procedures is key for any medical device manufacture

How to Choose a Translation Vendor

Learn important strategies for selecting a translation vendor. Topics include:

  • Understanding translation pricing
  • Translation memory
  • Regulatory considerations
The Argo Team delighted me and made my whole team look good. Work with Argo. You will not be disappointed. Joe Hage

DIRECTOR OF MARKETING, CARDIAC SCIENCE

Interested in launching an RFP for translation?

Download a sample RFP template you can use to immediately qualify a prospective translation vendor.

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Our expert translators start as soon as you need them, working within timelines that fit your needs.
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