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Preformulation
Prior to embarking on a formulation design program, we analyse the API for its physicochemical, biopharmaceutical, particulate and bulk properties. In doing so, we adhere to our philosophy of phase-appropriateness, meaning we collect increasingly detailed information as a compound progresses through development.
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API-sparing
Our miniaturized protocols enable the collection of detailed information while consuming only mg-quantities of API
Phase-appropriate
We work closely with our customers to understand their needs and collect the right data at the right time.

Rapid turnaround
Our agility and specialization enable us to work faster than generalist CDMOs. No work package is too small for us.
Our preformulation services
  • Physicochemical
    Solid form screening and selection
    Solubility
    pKa
    Log P
    Melting point
    Chemical stability
    (heat, oxidation, light, pH)
    Hygroscopicity
  • Biopharmaceutical
    Solubility in biorelevant fluids
    Stability in biorelevant fluids
    Dissolution rate
    Permeability
    Metabolic stability
  • Particulate and bulk
    Particle size
    Particle morphology
    Flow properties
    Density
    Compressibility
    Wettability
    Excipient compatibility
Free project consultation
If you would like to learn more about our preformulation services, you can reach out to one of our experts here. We are happy to make a gap analysis of your current preformulation data package and suggest appropriate follow-up experiments to inform your formulation development project.
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