VxP Pharma provides development and manufacture of lyophilized products for both small and large molecule programs. We also provide services for your pre-clinical/tox studies with cGLP manufacturing of liquid and lyophilized drug product. Whether you are in early development and needing lyo cycle development and optimization, or needing full GMP manufacturing, our VxP team can help guide your project from concept to the clinic, and to market.

Some areas of specialization include:

Development Services

  • Low Temperature Thermal Analysis
  • Product Development
  • Cycle Design/Refinement
  • Finished Product Testing
  • Aqueous/Organic Solvents
  • Pilot Plant Scale-up

Preclinical/Tox Materials (cGLP) and Clinical Manufacturing (cGMP)

  • Sterile Bulk and Drug Product
  • 2cc to 160cc Presentations
  • 13-28mm Closures
  • Temp controlled compounding/filling
  • US and EU Compliant
  • Cytotoxic/Highly Potent Capabilities