Medical device documentation (user manuals, instructions for use, labelling, technical specifications, maintenance instructions etc.)

Products in medical devices are regulated, and device documentation must be provided in local language in many jurisdictions.

Patient / clinician information guides, patient diaries, questionnaires, surveys, PROs (Patient-Reported Outcomes)

These are used both for patient care (e.g. instructions) and in research / clinical trials (e.g. diaries, outcome measures).

Regulatory / Pharmaceutical documents (e.g. registration dossiers, product labelling, patents, summary of product characteristics, packaging & inserts)

Whenever a pharmaceutical product is being approved, launched, or sold in another market, these documents have to be translated.

Informed Consent Forms (ICF), Investigator Brochures, Clinical Study Protocols, etc.

Used in clinical research / pharmaceutical trials. Entities sponsoring trials need documents translated for regulatory submissions, participant consent, local ethics committees.

Medical records / reports

These include hospital reports, physician’s notes, patient histories, discharge summaries, laboratory test results etc. A frequent need arises when people move, travel, for immigration, for insurance, for second opinions.

Other Document Type

For all other document types please select this option