Clinical Pharmacology

Need confidence that your molecule will move into clinical testing quickly and safely?

CPhI North America

April 24-26, 2018, Philadelphia, PA, U.S.

Meet us at CPhI North America in Philadelphia to discuss any formulation development, clinical and commercial manufacturing requirements you may have.

Quotient Sciences US manufacturing facility is located in Boothwyn PA, less than 30 minutes’ drive from the CPhI venue. If you would like a tour of our state-of-the-art facility, please contact us to make arrangements.

We'll be located at booth #1339.

Why speak with us?

  • Discuss Quotient’s Translational Pharmaceutics® platform which integrates CDMO and CRO services to significantly accelerate timelines and reduce costs
  • Review your formulation development and product optimization requirements with our expert team
  • Understand how adaptive real-time GMP manufacturing and flexible batch sizes can be tailored to the clinical design
  • Make plans to develop scalable manufacturing processes from Phase I to commercial supply

Receive updates on Quotient’s global capabilities:

  • Expanded high potency containment facilities in the U.S. and U.K.
  • New API characterization and pre-formulation capabilities
  • Comprehensive solubilization technologies for poorly soluble molecules
  • End-to-end support for pediatric development programs

If you would like to meet us there, please email Tobi Williams, Director, BD (U.S.).

Ask us a question