As a medical device manufacturer in a high-growth, globalised industry, you need a strong, quality-driven translation services partner with expert resources and the ability to scale up as and when needed.
Our team of qualified translators will quickly and accurately translate all your medical device content – one of your key growth drivers – so that it is accessible to patients and users in different markets.
We will ensure that documentation for medical devices in the approval pipeline meets the strict language and translation criteria enforced by international governmental bodies and in newly drafted regulations.
We can offer technical writers and translators to support you with the following types of documents:
- Clinical study protocols
- Clinical study report forms
- Field safety notices (FSNs)
- Operating, installation and maintenance manuals
- Instructions for use/Directions for use (IFU/DFUs)
- Informed consent forms
- Packaging and labelling
- Patient questionnaires
- Product catalogues
- Scientific articles