UPM has extensive experience and expertise in the development of solid oral dosage forms, including controlled and immediate release formulations. Formulation development capabilities include blending, high shear granulation, fluid bed granulation, extrusion-spheronization, roller compaction, bi-layer compression, mini-tablets, encapsulated tablets and beads, coated tablets. UPM also has expertis with development, testing, formulation and manufacture of semi-solid drugs, including creams and ointments.
Formulation development has been one of the key services UPM has offered since its inception at the University of Maryland. Our experienced and professional scientists thoroughly enjoy providing industry standard and unique solutions for our clients and their respective drug development programs. UPM’s formulation evaluation services for solid oral and semi-solid creams and ointments include:
The R&D group works closely with the analytical group to ensure the appropriate testing, method development, and timeliness is maintained for each Client development program.