Pre-formulation solubility,stability evaluations,Comprehensive excipient screening,Prototype development,Formulation optimization and finalization,Supporting documentation and data package

cGMP Manufacturing

Once a clinical formulation is developed, the decision where to manufacture clinical supply is critical to maintaining product development timelines and ensuring product quality. Our specialization in Phase I/II manufacturing provides a unique advantage to our clients seeking to manufacture clinical supply material using current Good Manufacturing Practices with necessary regulatory compliance. At ECI Pharmaceuticals, focus on early-phase development enables us to be flexible and responsive to your manufacturing needs. Clients can depend on on-time delivery of clinical trial materials and trouble-free technical transfer for Phase III and commercial scale-up.
  • Pre-formulation solubility and stability evaluations
  • Comprehensive excipient screening
  • Prototype development
  • Formulation optimization and finalization
  • Supporting documentation and data package