Finished Dosage Forms vs. APIs: What’s the Difference in Pharmaceutical Manufacturing?
Explore the key differences between Finished Dosage Forms (FDFs) and APIs in drug development and manufacturing.
Explore the key differences between Finished Dosage Forms (FDFs) and APIs in drug development and manufacturing.
We’re delighted to share that Upperton has officially been accredited as on of the Sunday Time Best Places to Work 2025
We’re delighted to announce that Upperton has officially been accredited as one of The Sunday Times Best Places to Work 2025
Our Approach Project Initiation and Onboarding We typically initiate projects within two to three weeks of proposal acceptance. During this time, we manage project onboarding and procure any necessary materials. Our analytical team plays a crucial role in onboarding new methods, confirming their suitability, and ensuring readiness for the subsequent stages of your project. This … Read more
Upperton continues growth with appointment of Michael Mellor-Clark as Chief Commercial Officer.
Discover more about our team. In this Spotlight, meet our Director of Pharmaceutical Sciences, Laura Mason, on her journey with Upperton.
Upperton is proud to announce its recognition as the Champion Award Winner in the Small Molecule Dosage Form category at the CDMO Leadership Awards.
We are delighted to share that we have been shortlisted as a finalist in the Excellence in Innovation category at the Medilink Midlands Business Awards 2025.
Addressing CMC considerations early in the drug development process is vital in the successful creation of a pharmaceutical product.
Addressing CMC considerations early in the drug development process is vital in the successful creation of a pharmaceutical product.