We have extensive experience in the translation of documents that are usually managed by the areas of Regulatory Affairs, Research and Development, Control and Quality Assurance, Marketing, Tenders, etc., such as:
ISOs, GMPs, Certificates for Foreign Government, Pharmacopoeia (US, Ph Eur, JP, etc.), Certificates of Analysis, Brochures, Safety and Efficacy Studies, Stability Studies; Health registrations; Pharmacovigilance Documents, Product Characteristics Summaries (Technical Data Sheets), Clinical Trial Documents, Marketing Applications, OTC Renewals, Documentation of New WFIs, Drug Registration Records; Research reports, etc.
This is why we already have formats and terms validated for this type of documents, which allows us to work at the speed that fits your needs.