One partner. Every phase. Visit booth 6A2 at CPHI Milan 2026 to streamline drug development.
Clinical timelines rarely wait. Delays in development can affect funding, milestones, and patient access.
Thermo Fisher Scientific's OSD Express solutions are designed to compress timelines for early oral solid dose development and technology transfer, helping you move efficiently from development through clinical supply while maintaining quality and financial goals.
Powered by our optimized processes, parallel workstreams, and deep technical and regulatory expertise.
Competitive pricing, flexible financial options, and efficient timelines without compromising quality.
Robust global network, decades of experience, and a strong history of on-time, high-quality delivery.
What’s in scope?
Final deliverable: GMP clinical batch in 25 weeks* from receipt of customer’s API and API reference standard
Site location: Bend, Oregon
What’s in scope?
Final deliverable: GMP clinical batch in 21 weeks* from receipt of customer’s API, API reference standard, and drug product for analytical transfer
Site locations: Bourgoin, France, Cincinnati, Ohio, Manati, Puerto Rico, Toronto, Canada, Whitby, Canada
*Actual timeline may vary and is a good faith estimate based on best available data. Timeline begins on Thermo Fisher’s receipt of API and ends on release of CTM by Thermo Fisher.
Tell us about your OSD program and we’ll route your request to the right team.