UPM Pharmaceuticals can perform investigations of the physical and chemical properties of an API alone or in combination with other drug substances or exipients. These studies provide valuable data and information so our experienced formulators can develop the most stable and bioavailable dosage forms. The formulations that UPM develops for its clients can be scaled up for clinical and ultimately commercial supply.
UPM’s Preformulation capabilities:
Particle Size Analysis(by laser)
Differential Scanning Calorimetry(DSC)
Thermal Gravimetric Analysis(TGA)
Osmolality
Coulometric Moisture Analysis
HPLC with ELSD
Dynamic Moisture Sorption
Moisture Sorption Isotherm
Surface Tension
Heat of Solution
Ph/PKa
Flame Photometry
Solubility
Microscopy
Equilibrium Solubility in Various Solvents
Exipient Interactions / Compatibility
Melting Point
Glass Transition
Decomposition
Purity Analysis
Crystallinity
Polymorphism
Stability
UPM’s key Pre-Formulation equipment includes:
Thermogravimetric Analyzer
Differential Scanning Calorimetry
Particle Size Analyzer by Laser
FT-IR
Static Humidity Chambers
R&D Stability Chambers
Flodex
Bulk/Tap Density
Sonic Sifter
Powder Dispenser
Key advantages to working with UPM’s team:
Extensive equipment train to carry out essential testing
Comfortable with API sparing techniques
Experience in method development and transfer techniques
Dedicated team of analysts, formulators, and manufacturing associates who will work closely together from early stage development to GMP scale up
Peer-to-peer communication on a consistent basis
On site scale up for clinical and commercial supply
Data and client confidentiality from relationship on set
Newsletter Signup
This website uses cookies to ensure you get the best experience on our website. Learn more