We at Mynnaf Translations are specialists in the translation and back-translation of all clinical trial-related literature, regardless of their design or developmental stage (stages I to IV), including:
- Study protocols
- Informed consent forms (ICFs)
- Correspondence with regulatory agencies (BfArM, CCMO, FAGG, ANSM, Swissmedic, etc.)
- Investigators’ brochures (IBs)
- IRB/Ethics committee-related correspondence
- Pharmacovigilance reports/PSURs
- Case report forms (CRFs)
- Patient-reported outcome (PRO) questionnaires
- Adverse event reporting
- CMC dossiers
Many of our translators have a background in working for CROs and pharmaceutical companies throughout Europe, and we strive to match each individual translation requirement with the most appropriate translator.
Why not use our request form for more information or any translation enquiry you might have?