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