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OUR SERVICES
Preformulation
  • Aqueous and pH Solubility
  • Drug-excipient compatibility
  • Physicochemical properties
  • Polymorphisms
  • Thermal properties
  • Particle size and morphology
Formulation
  • Immediate release tablet
  • Modified release tablet
  • Orally disintegrating tablet (ODT)
  • Sterile powder and solution
  • Lyophilized powder for injection
  • Semi solid dosage form: Cream, Gel
  • Analytical method development
  • Analytical method validation
  • Quality control of raw materials and finished products
  • Stability test in accordance with ASEAN guidelines
    - Accelerated condition : 40 oC ± 2 oC/ 75% RH ± 5% RH
    - Long term condition : 30 oC ± 2 oC/ 75% RH ± 5% RH
    - Long term condition : 25 oC ± 2 oC/ 60% RH ± 5% RH
    - Stability condition for semi-permeable containers
  • Pharmaceutical equivalence test
  • Bioanalytical method development
  • Bioanalytical method validation
  • Bioanalytical test
  • Bioequivalence study
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