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
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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