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Locations / CDMO Clinical Manufacturing / PA – Philadelphia

Philadelphia, PA

Drug development services from this site advance candidates from early pre-formulation and tox studies to an IND filing and on through the clinical phases. Our GMP clinical supplies manufacturing capabilities include oral solid/liquid and topicals capabilities, and clinical packaging and kitting for a variety of molecules/dosage forms.

Contract Development Manufacturing Organization (CDMO)

  • 33,000 ft² GMP Clinical Manufacturing Facility
  • Providing Services for More Than 20 years

Core Services:

  • Small Molecule Formulation Development, Preclinical and Manufacturing
    • Manufacturing: Tox supplies – Phase I/II Clinical Supplies
    • Tablets, Capsules, Liquids, Suspensions, Topical Creams, Gels, Ointments
  • Full Analytical Support
  • Controlled Substances & Potent Compounds
  • Solvent Processing
  • Solubility Enhancement: Spray-drying, Nano-suspensions, Hot-melt extrusion
  • Drug Product Release
  • ICH Stability Studies
  • Batch Sizes:
    • Gram scale to 50kg for solid dose
    • Gram scale to 125L for liquid and topical doses