Search Thermo Fisher Scientific
- Order Status
- Quick Order
-
Don't have an account ? Create Account
From drug production to commercialization and post-marketing approval studies
With our Combined CDMO and CRO—“CRDMO”—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 shared accountability 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 CRDMO 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 accountability, 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.
