Development
Bioequivalence Test
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.
