Upperton offers analytical services designed to support the development, monitoring, and quality control testing of pharmaceutical products. Our analytical team focus on understanding the physico-chemical properties of active pharmaceutical ingredients (APIs), as well as identifying potential stability challenges and excipient incompatibilities that may arise during product development.
Upperton uses a variety of techniques, including Differential Scanning Calorimetry, X-ray Powder Diffraction, Thermal Gravimetric 网曝门, microscopy, and Fourier-transform Infrared Spectroscopy, to gain insights into the behaviour of APIs. This forms the basis for supporting FIH studies and product development.
In terms of stability testing, Upperton integrates ASAPprime庐 into its development programs. This accelerated stability testing provides early indications of potential stability issues, allowing for faster decision-making to save time and resources.
By employing a wide range of techniques and offering comprehensive analytical support, Upperton helps clients mitigate risks, improve product performance, and ensure quality throughout the drug development cycle.