We have been committed to the translation of new drug application dossiers for more 10 years:

Documents of drug substances and drug products (including drug manufacturing processes and specifications), pre-clinical pharmacology and toxicology studies, Phases I/II/III clinical study protocols, clinical trial reports, clinical safety and efficacy studies, clinical pharmacological studies, clinical pharmacokinetic studies, periodic safety update reports, investigator’s brochures, package inserts, and other medical or pharmaceutical documents.