Bioequivalence Test

CR Medicon has created an integrated bioequivalence test platform to help our clients achieve rapid development.

Integrated Services & Advantages

  • Drawing from our extensive BE experience, quickly create high-quality dossiers required for testing, such as clinical trial plans, etc.
  • With multiple well-coordinated Phase I Centers, conduct BE trials of varying sizes and difficulties as well as enabling quick project initialization and rapid subject recruitment
  • Our own biological sample analysis and testing lab, fully meeting NMPA and FDA GLP requirements, enables rapid methodological establishment. Running with high-sensitivity analytical instruments, we are able to complete BE tests meeting or exceeding clients’ requirements.
  • An integrated service system enables quick collaboration of various business teams to accelerate the project progress
  • A statistical analysis process specially optimized for BE tests generates statistical analysis reports in short time.