To succeed in today’s complex drug development environment, you not only need speed, efficiency, and effectiveness, but also a trusted CDMO partner you can depend on. Thermo Fisher Scientific offers industry-leading pharma services through our Patheon™ brand, offering an integrated global network of scientific, technical, regulatory, and quality experts who are committed to helping you deliver medicine to patients faster. We believe that doing this successfully not only requires science, technology, and world-class expertise, but also a strategic partnership—bonded by key elements such as trust, communication, and collaboration.
With more than 60 locations around the world, we are committed to providing integrated, end-to-end solutions across all phases of development. Our pharma services include API, biologics, viral vectors, cell therapies, formulation, clinical trials solutions, logistics services, commercial manufacturing, and packaging. We couple our scientific and technical excellence in these areas with a strategic partnership to provide customers of all sizes access to a global network of facilities and dedicated experts across the Americas, Europe, Asia, and Australia.
60 locations
Thermo Fisher Scientific pharma services has over 60 locations across 24 countries
463,000
463,000+ clinical shipments completed in 2022, providing the tools needed to execute clinical trials to accelerate the delivery of safe, high-quality medicines to patients
30 purpose-built GMP facilities
Global clinical trial service network comprised of 30 GMP compliant facilities in support of clinical trial supply chain services
Whether you need to create or source your active pharmaceutical ingredient (API), design the ideal formulation, scale to your next clinical trial milestone, develop a supply chain strategy, ensure production continuity, or deliver a successful commercial launch, we meet you where you are.
Our 642,000 sq ft campus in Monza, Italy is a center of excellence for sterile manufacturing. It features a unique co-location of mRNA manufacturing capabilities with LNP and fill finish services to help streamline your processes and mitigate risk.
Capabilities: Steriles, mRNA
Our Greenville, NC facility is a large, multipurpose pharmaceutical manufacturing and packaging campus. This site provides both solid dose form manufacturing and packaging and sterile dose manufacturing, filling and lyophilization of both biopharmaceuticals and small molecules.
Capabilities: Steriles
Our Ferentino facility is 14,034 m2 (151,061 ft2), specializing in integrated sterile liquid and lyophilized product development and commercial manufacturing, including high potency products and LVP.
Capabilities: Steriles
Our Groningen site specializes in cGMP for (pre)clinical and commercial manufacturing, including mammalian cell culture manufacturing, scale up and cGMP manufacturing of recombinant proteins and monoclonal antibodies.
Capabilities: Biologics
Our Lengnau facility is a state-of-the-art multipurpose biomanufacturing site in the heart of Europe. This 1.5m sq. ft. facility leverages highly flexible bioproduction technologies, including stainless steel up to 12,500 L bioreactor capability, providing a pathway from development to large-scale production as your manufacturing needs evolve.
Capabilities: Biologics
Our 44,000 sq ft state-of-the-art facility is adjacent to numerous oncology hospitals in the Bay Area and ~15 minutes from the San Francisco International Airport. Equipped with individual, user-configurable cGMP-production suites, we can support multiple cell lines/multiple products simultaneously due to our unique dedicated HVAC system for each suite.
Capabilities: Cell Therapy Manufacturing Services
Allentown is our largest ambient and cold packaging, storage and distribution facility for clinical trials. The site has expanded services to include commercial packaging with serialization, offering primary packaging of oral solid dose for blister packs and bottles, with additional secondary packaging services for syringe, pre-filled syringe, pen, autoinjector assembly and labeling.
Capabilities: Clinical supply solutions
Our Basel site offers a comprehensive service line supporting all aspects of clinical trial supply - primary and secondary packaging, labeling, regulatory support, distribution, returns and destruction, and comparator sourcing. Additionally the site supports cold chain supplies management and has in-house engineering capabilitites for tooling, equipment customization, and production automation.
Capabilities: Clinical supply solutions