Please find details of our latest downloadable Fact Sheets below and fill out the form to gain access to the them as PDF’s.
Upperton provides an extensive range of analytical techniques to generate critical product data from the early stages of development through to QC testing of clinical supplies. This data guides formulation development and is used to assess stability and evaluate the performance and quality of the final dosage form.
Upperton can offer clients expert preclinical and clinical formulation development of oral solid
dosage (OSD) forms; from early feasibility, right through to clinical manufacture. Formulations
can range from simple powder in bottle/sachet for reconstitution to more complex capsules and tablets.
Producing a successful pulmonary drug product requires expertise in formulation
development, particle engineering and device selection. Inhalation product testing capabilities are also vital, to ensure that the developed product can effectively deliver the target dose into the correct region of the lung.
Spray drying is a simple yet incredibly flexible technology that can transform liquids into
powders in seconds. Manipulation of feed solution composition and process parameters allows the creation of spray-dried powders with a range of physical and aerodynamic properties.
Upperton’s expertise covers a wide range of pharmaceutical technologies, from traditional
powder blending, granulation, tabletting and capsule filling to more advanced enabling
technologies such as spray drying and jet milling, for bioavailability enhancement, and particle
engineering for targeted pulmonary and nasal delivery.