Q-Trials offer Document Translation and Validation Services for health care companies and Clinical Research Organizations.
Our translation department experly handles medical texts performing translation, adaptation, and verification of study materials, with a focus on informed consent forms and other patient materials required for clinical studies. Our longstanding experience and know how regarding language level and the correct use of medical terms within these special documents, as well as our familiarity with the medical jargon, ensure we can deliver top quality products within excellent timelines and competitive pricing.
Our subject proficient translators are selected from medical proffession thus their knowledge of the clinical trial arena is inherent.
We routinely translate:
- Informed Consent Forms
- Patient Diaries
- Patient Questionnaires
- Instructions for Use (IFU)
- Package Inserts and Product Labels
- Patient Information Leaflets
- Ethics committies and MoH application & approval forms
The majority of our medical translation work focuses on the Translation, Verification and Adaptation of study documentation written in English, Russian, Hebrew, and Arabic, among others.
Project management ensures documents are proofread and verified independently against the original document and in line with a strict Quality Control process and privacy guidelines.
Our cost-effective, accurate and timely document translation services yield a final document translated and verified, certified and ready for EC approval and for use by the subject.