Clinical Trial Management
When clients need translations for clinical trial documentation, they can rely on RWS Life Sciences – the leading and trusted authority in translation – to get it done right the first time, every time.
Translations are an essential component of moving global clinical trials forward. Our expert knowledge and exclusive focus on the life sciences industry allows our team to handle any translation request with confidence.
Clinical trials are rarely static, and our clients regularly come to us with rush translation requests, shifting timelines and revisions from ethics committees. Our procedures are flexible, so we can deliver on time and in the most cost-effective manner.
Our singular focus in translating documentation for the life science industry has made us experts in analyzing clinical trial documents so we can deliver the most appropriate translation method:
- Protocol Synopses
- Informed Consent/HIPAA/Assent Forms
- Investigator Brochures
- Patient Questionnaires
- Patient Diary/Event Log
- Patient Records
- Case Report Forms (CRF)
- Clinical Outcomes Assessment Questionnaires (COAs/PROs)
- Adverse Event Reports
- Ethics Correspondence