Translation for the medical industry.
The pressure is on. But we can help. Pressures on regulated industries has increased. Translation is a must to bring a medical product to a foreign market. Traceable Standard Operating Procedures (SOP's) are necessary to comply with the FDA, EU Medical Device Directives (MDD, AIMDD and IVDD) and other national and regional directives.
Reduce costly reviews and the risk of recall. And stay competitive all while complying with international and regional directives.How? With Argo's Regulatory Compliance Platform (RCP). The RCP supports the full translation and localization life cycle. It provides secure online access and reporting for each completed project detailing all project contributors. The system also provides easy auditing with scanned and stored credentials for each linguist involved.
Related Blog Posts:
Argo Case Studies:
"The Argo team delighted me and made my whole team look good. Work with Argo. You will not be disappointed."