International life science companies face a maze of complex regulatory requirements in each stage of the pharmaceutical or medical device development cycle to bring their products to market or qualify for fast-tracked clinical trials in each target country. PA Localisation’s skilled language professionals have extensive experience in translating multilingual regulatory labels, summaries of product characteristics (SmPC), product information leaflets, CTD/eCTD modules, patent filings, clinical trial management materials, scientific treatises, product licensing, package inserts, and other related technical documentation. Our precise, rapidly-delivered translations are backed by state-of-the-art technology and always adhere to the highest quality and data security standards in your documents, including UK, US, and European Commission privacy regulations.