Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon.
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. Learn more about Thermo Fisher’s Supplier Diversity Program.
Thermo Fisher Scientific provides industry leading pharma services solutions for drug development, clinical trial logistics and commercial manufacturing to customers of all sizes through our Patheon brand.
With more than 55 locations globally, we provide our clients with integrated, end-to-end capabilities through all phases of development, including API, biologics, viral vector services, formulation, clinical trial solutions, logistics services and commercial manufacturing. We give pharma and biotech companies of all sizes access to a fully integrated global network of facilities across North America, South America, Europe, Asia, Africa 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, viral vector expertise, 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 17,000 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 800 clients, we’re rapidly turning pharmaceutical possibilities into realities.
Contact us to discuss your upcoming development, clinical trial or manufacturing project with our experts.
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