At CIRION, your development and validation projects are in good hands with our scientific team. Our research specialists have the ability to design, develop and validate customized methods and laboratory assays in compliance with GLP requirements. Method transfer of your assays is also possible through our rigourous method transfer protocol.
We have extensive experience in laboratory analysis for human and non-human biological fluids and tissues and are committed to the advancement of science by developing and validating new analytical methods and processes and improving existing assays in a GLP environment.
In addition, we have established a network of clinical scientific advisors to provide support on advanced clinical trial applications for specific projects in the fields of hematology, microbiology, cytogenetics and pathology.
Assay development and GLP validation capabilities
To support your clinical development projects, our scientific team will contribute to your product development by sharing extensive experience in:
- Biologics / Biosimilars (Large Molecules)
- Cell Biology
- Molecular Assays