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From drug production to commercialization and post-marketing approval studies
With our combined CDMO and CRO expertise, Thermo Fisher Scientific supports commercial drug manufacturing, GMP testing, global logistics, post-approval regulatory services, and safety studies, and provides extensive RWD/E registry information, and product life-cycle consulting.
Our unique, fully end-to-end approach ensures collaboration across commercialization, production, and post-approval processes, helping to enable increased speed, simplicity and scalability.
Drug production, commercialization, and post-approval service for your drug development journey
Select a commercial drug manufacturing, clinical research, or laboratory service in the table below to learn more about how we can help you during your new drug commercialization process and beyond.
In-House Manufacturing Solutions
Building an ecosystem of connected CDMO and CRO services to support your asset development
We’ve forged a unique approach backed by decades of experience and know how.
Central to this approach is a commitment to ensuring that across drug substance manufacturing, drug product manufacturing, clinical supply, and clinical trial research there is a collaborative approach, with joint program management and data transparency—leading the way to exceptional outcomes.
