Translation, transcription, editing, proofreading, localisation and interpreting for medical, clinical and research-related work.
Around 95% of our work is clinical and health research. We understand the terminology, the documentation and the deadlines that come with ethics submissions, trials and publication.
Clinical and medical research documents: informed consent forms, ethics submissions, trial protocols, patient information leaflets, case report forms, questionnaires, surveys and research articles for publication.
Clearer, more consistent text, reviewed by an experienced editor.
A final check before your document is submitted, published or filed.
Adapting content for a specific language and audience, so it reads naturally in the local context.
Accurate written records of interviews, focus groups and proceedings.
Spoken language support for interviews, meetings and research sessions.
Every project follows the same four steps, with security and consistency built in.
We review industry-specific terminology and your glossaries before the project starts.
Subject-matter linguists translate into their native language.
A senior editor proofreads the text against agreed quality criteria.
Automated and manual checks before the file reaches you.
Client files are processed on encrypted cloud servers and handled under non-disclosure agreements.
Translation memories and client glossaries, using CAT tools such as SDL Trados.
Exempted Micro Enterprise, Level 1 Contributor, 135% procurement recognition. Certificate available on request.