Sterile Formulation Development

With over 20 years of experience, PCI’s strength lies in our ability to manage products with unique challenges ranging from small molecules presenting with solubility issues or a labile molecule that is only stable as a liquid presentation for a short time.

Whether you are developing a liquid or lyophilized dosage form, we understand that speed and flexibility are critical to the success of your development program. We can screen multiple experimental formulations in parallel to expedite the formulation development phase of your program to enter the sterile fill-finish step. We focus on developing reproducible, scalable, and commercially robust processes, delivering time and cost efficiencies.

Our dedicated team of specialists will be happy to discuss our Sterile Formulation Development Services with you. Contact us on +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email

Start your PCI experience today.

Rely on our sterile formulation development services. Your drug product destination means the world to us.

Always growing and continually advancing, we support you from early-stage development through commercialization and beyond, and with 6000+ people in 30 global GMP facilities, we are always near.