We all know that medical technology is regulated by strict regulations and even a small error can lead to user errors, deterioration of the brand’s reputation and increased costs. Considering all these,

– We ensure your projects are handled by linguists with an expertise in medical translation and a good knowledge of relevant terminology and up-to-date regulations (e.g. EU Regulation 2017/745 on medical devices).

– We have the editing  phase performed by editors experienced in the medical field.

– If required, we have our medical experts for the proofreading process, as a result of which we ensure that your content complies with the medical literature.

– We effectively use computer-aided quality assurance tools (QA tools) to attain consistency and completeness in the texts produced, and we deliver your projects accurately in time. We complete all these steps according to the criteria set forth in the ISO 17100 standard specific to the translation sector.

 With our help, you can market your products safely within global reach.