Biomedical Translation
Wide experience in translating scientific documents, including translation of documents related to Clinical Trials, Registry and Launching of new pharmaceutical drug products, management of drug safety, publications, manuals and guidelines. The process of biomedical translation includes the translation, correction as well as an accurate interpretation of the texts in order to preserve the original context.
Clinical Trials Documentation
– Protocols and Amendments
– Reports
– Patient records
– Case Report / Record Forms
– SOPs
Documentation for Sales and Marketing
– Product Monographs
– Product Technical Information Questionnaires
– Promotional Material
– Brochures
Documentation for Product Registration
– Technical Dossiers
– Expert Reports
– Summary of Product Information / Company Core Data Sheet
Scientific Documentation
– Scientific manuscripts
– Abstracts, posters
– Presentations
Quality Assurance
– Manuals and guidelines
– SOPs
– Audit Reports
Pharmacovigilance
– Periodical Safety Update Reports
– Expert Reports
– Adverse Events / Drug Adverse Reaction Expedited Reports
– SOPs