Pharmaceutical Analysis and Stability Testing

Measuring the stability of pharmaceutical and bioanalytical products continues to present new challenges to our customers. With our GMP/ICH compliance programs, Toxikon has immense analytical expertise. We offer cost effective solutions to fulfill the requirements for drug substance, drug product, and delivery systems.

Toxikon's analytical services include:

• Evaluation of residual solvents
• Identification of impurities and degradation products
• Method development - includes stability indicating assays
• Method validation
• Photostability testing
• Post-approval stability trials
• Stability trials for
  • Clinical applications
  • Formulation development
  • Product license applications

Our stability services include all stages of drug development, from the beginning stages of research and development to complete studies for submission requirements.