Medical translation is the translation of regulatory, clinical, training documentations of the pharmaceutical, medical devices or for healthcare fields. In order for local clinicians and patients and regulatory representatives to be able to read, regulatory approval submissions also have to be translated as well. Apart from linguistic skills, it requires training and knowledge in specific subject matter in order to translate medical content. This is because of the highly technical, sensitive and regulated nature of medical texts.
For the above reasons, we only employ former healthcare professionals for our translation jobs. We've been translating medical documents for biotechnology companies, pharmaceutical companies, medical device manufactures, and clinical research organizations.
The types of medical documents that we do translate are listed below:
Adverse events, case report forms, clinical rules, clinical trials, contracts, data sheets, dossiers, drug registration documents, manufacturing process specifications, master batch records and deviation reports, marketing collateral, package inserts and labels, pharmacological studies, product labels, production manuals, questionnaires, regulatory documents, SAE and SOP procedures, scientific journal articles and corporate websites
Contact our team of medical translators now to discuss your requirements, and see how successfully we assist you to complete your task.