Translation into languages for traditional and emerging clinical trial locations.
Frequently translated documents:
- Clinical study protocols
- Protocol synopses
- Informed Consent Forms (ICFs)
- Patient/Doctor information sheets
- Investigators Brochures
- Trialists’ CVs
- Ethics Committee Letters
- Case Report Forms (CRFs)
- Adverse Event Report (AER) forms
- Insert & label text
- Appointment, reminder, follow-up cards etc.
- Patient Reported Outcomes (PROs)/Quality of Life Instruments
- Patient diaries and questionnaires
- Directions for Use
- Pharmacy manuals
- Interim/final reports