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From the earliest stages of development to final distribution to your patient, together, we can make an impact. Thermo Fisher Scientific’s global network of pharmaceutical development and manufacturing facilities are among the most technologically advanced and cGMP compliant available. With sites in more than 30 countries world-wide, we provide end-to-end capabilities across all phases of development, including API, biologics, viral vectors, cGMP plasmids, formulation, clinical trials solutions, logistics services and commercial manufacturing and packaging. We give pharma and biotech companies of all sizes instant access to technical experts across the Americas, Europe, Asia, Africa, and Australia. Through our Quick to CareTM program, we provide drug development and clinical services that are tailored to fit your unique drug development journey.
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