A scientist uses a pipette to add liquid to a 96-well plate, with wells filled with different colored solutions for high-throughput experiments.

Pharmaron has expertise with biophysical screening, which is highlighted by our experience with platforms such as surface plasmon resonance, biolayer interferometry and liquid chromatograph-mass spectroscopy. Our analytical development services interrogate the composition and formulation of the developing biologic to ensure the highest level of compatibility and translatability to GMP scale-up.

Leverage our experience and state-of-the-art technologies, such as chromatography and automated capillary electrophoresis systems, to extensively characterize the developing biologic to meet the standards of regulatory authorities.

A scientist in protective gear works with an automated system for in vitro biology studies, preparing samples in a sterile laboratory environment.

Characterization Capabilities

  • Biophysical screening
    • Interrogation of the molecular interactions for developing biotherapeutic assets through a panel of services, including label- and label-free technology platforms
  • Biochemical characterization
    • Examination and definition of biochemical traits for the biotherapeutic through analytical methods to measure and quantify cellular processes and biochemical/phenotypic therapeutic responses
  • Analytical characterization
    • Analytical procedures intended to test and quantify specific characteristics of biologics against predefined acceptance criteria

Learn more about Pharmaron’s in vitro biology services