МЕДИЦИНА И БИОЛОГИЯ
Contract Research Organizations
Compliance with strict international regulations creates an urgent need for precise translations of clinical documents, completed with an in-depth knowledge of the industry and global markets.
CROs conducting clinical trials internationally have to conform to the requirements of the FDA, EMEA and other regulatory organizations and ethical committees. Regulators require that the patient recruitment materials, Informed Consent Forms (ICF), clinical protocols and other documents be in a language that is clearly understood by the people participating in the clinical studies.
Time and again, Language Connections has proven itself to be a reliable partner in such ventures. We have provided expert multilingual support to CROs, translating product labeling, clinical trial documentation, patient recruitment materials, as well as marketing and legal documents.
We work with some of the most successful pharmaceutical companies around the world, as well as numerous biotechnology and medical device firms. We translate into over 100 languages in a timely, cost-effective way, and work in a variety of visual and audio media, in addition to hard copy and text files.
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