Thermo Fisher Scientific Inc. is the world leader in serving science, with revenues of more than $20 billion and approximately 70,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity. Through our premier brands—Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services—we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services.
Our Supplier Diversity Program provides qualified certified small and diverse businesses with opportunities to become a preferred vendor for Thermo Fisher Scientific. We recognize the importance of valuing the diversity of our employees, and all whom we do business with is an integral element of our corporate culture. We are committed to ensuring that we embed an inclusive culture in all our business practices and actively seek to maximize business opportunities for certified small and diverse businesses.
Thermo Fisher Scientific’s Patheon and Fisher Clinical Services brands have come together to provide industry-leading pharma services solutions for drug development, clinical trial logistics and commercial manufacturing to customers of all sizes. With more than 40 locations around the world, the company can provide integrated, end-to-end capabilities across all phases of development, including API, biologics, formulation, clinical trials solutions, logistics services and commercial manufacturing. We give all sizes of pharma and biotech companies, including the very smallest, instant access to a fully integrated global network of facilities across North America, Europe, Asia and Australia. Our global leadership is built on a reputation for scientific and technical excellence. This includes specialized capabilities for highly potent and controlled substances, aseptic filling and lyophilization, complex formulations, solubility enhancement and difficult-to-manufacture APIs. We also offer integrated services for drug development that aligns development of drug substance and drug product in a coordinated drive toward proof of concept that can reduce development timelines. We have more than 12,000 scientific and professional staff and over 40 years of experience. As a leading global CDMO, we deliver unrivaled quality, reliability and compliance. Together with more than 400 clients, we’re rapidly turning pharmaceutical possibilities into realities. Contact us to discuss your upcoming development or manufacturing project with our experts.
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