When it comes to Compliance Documents and Submissions, you need a trusted expert in professional document translation and localization. One that understands your need to have materials translated to the highest level of accuracy—even under strict deadlines. One that knows the importance of handling patient data appropriately. In OmniLingua Worldwide, you’ll partner with a language services provider with more than 30 years’ experience. In fact, we help some of the largest medical device and pharmaceutical companies in the world meet stringent global regulatory and quality requirements.
Our translators know QRD templates, ensuring consistency and precision for the European Union market. In East Asia, OmniLingua was a pioneer with in-country translation teams in the early 1990s. We translate:
- Structured Product Labeling (SPL) experience
When it comes to European Union submissions, you can rely on OmniLingua to understand:
Active Implantable Medical Device (AIMD)
In Vitro Diagnostics Directive (IVDD) compliance when obtaining your CE Marking
Medical Device Directive (MDD)
Interested in partnering with OmniLingua Worldwide? Please contact us.