We have helped many of the world’s leading medical device and pharmaceutical companies in their successful submission of multiple IND/NDA/BLA/ANDA and other registration and application dossiers.

Pharmaceutical companies are required to submit large volumes of application dossiers to local regulatory authorities during the overseas registration and application process. Across all stages of drug development, including clinical trials, application dossiers are required to be professionally translated, to ensure compliance with regulatory requirements. EC Innovations is committed to providing you with high-quality, professional translation services, in a accurate and compliant manner, for your application dossiers.


Translation Project Process

Quality Assurance

Deeply aware of the importance of accurate translation to customers, the Life Sciences business unit at EC Innovations is committed to developing and refining quality assurance procedures tailored to the life sciences sector, including professional translation and editing, subject matter expert (SME) review, in-country review, language verification, desktop publishing, and language quality assessment (LQA), with the aim of consistently delivering high quality at low cost and with a short lead-time for every translation project.

We are among a handful of language service providers in the world holding ISO 9001, ISO 13485, and ISO 17100 certifications. We are also certified to comply with ISO27001 on data security.

Testimonials

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