Medical and Pharma Translation Solutions- Paspartu offers translation support in all stages of the medical product life cycle: clinical, regulatory, production, marketing, pharmacovigilance.
Medical translation is a highly regulated field that requires terminology precision, up-to-date technical knowledge, and familiarity with specific regulatory legislation, glossaries and instructions.
Paspartu has aquired vast expertise -over 500,000 pages translated since 2006- in the medical and pharma field alone, for key international medical device producers, biotech, life sciences and pharma companies worldwide.
Our medical translation team benefits from the involvement of regulatory professionals who are aware of specific country regulations and guidelines to be consulted when it comes to translating vital information, as well as of Subject Matter Experts employed in the revision phase of our Life Sciences documents.
Paspartu’s advantage in medical translation
translation, proofreading, back translation, harmonization of language versions, localization, interpreting, Quality Cross Check of running language projects, translation API for multilingual website management
We translate and localize for:
Clinical Research Organizations (CRO)
Original Equipment Manufacturers (OEM)
Contract Manufacturing Oragnizations (CMO)
Medical Devices Producers
Back translation for clinical trials documentation – At Paspartu we use back translation as a special quality control tool – for clinical trials documentation such as Patient Reported Outcomes, Informed Consent Forms, technical manuals and other highly sensitive documents where translation mistakes can cause major problems to the client, as important decisions regarding human health and safety are taken based on the translated texts.