Eurofins Optimed is a CRO with more than 30 years of experience in early phase clinical trial. We provide a complete range of services in drug, food and MD development and ensures the smooth and swift progress of your study at every step. From inclusion to study monitoring, from the conception of study documents to the final clinical report, from first-into-human to proof-of-concept, we provide full or custom-made services. Our own 60-bed clinical pharmacology unit has up-to-date equipment to ensure the success and the relevance of your study in various therapeutic fields, in healthy volunteers or patients. With a database of over 30 000 rigorously selected volunteers (questionnaire and medical examination), Eurofins Optimed can recruit in due time from a large pool of healthy volunteers and specific populations. The Quality Assurance policy in force at Eurofins Optimed will ensure that your clinical trials are performed with high levels of accuracy, reproducibility and security, in compliance with international standards (FDA, EMA, ICH, EFSA). Therefore, all studies can be presented in Europe and in the US for drug, nutrition, and medical device applications.
Phone: +33 4 38 37 27 40
E-mail: optimedsales@eurofins.com
Web: https://www.eurofins.com/biopharma-services/clinical-trials/
Add：1 rue des Essarts, 38610 Gières
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