Our contract research organization stands as your trusted partner, offering comprehensive preclinical method validation services under full Good Laboratory Practice (GLP) conditions to ensure the validity and reproducibility of your analytical methods.
Your Gateway to Validated Methods in a GLP Environment
With a team of experienced scientists and analytical chemists, we possess a wealth of expertise in designing, evaluating, and validating a wide range of analytical methods under full GLP compliance. Our large molecule bioanalytics experts currently develop and validate ELISA screening assays for anti-drug antibodies as well as titer assays to measure vaccine titers.
We adhere strictly to the highest standards of GLP regulations throughout the entire method validation process, ensuring the quality and integrity of your analytical methods. Our GLP-compliant method validation services include:
- A comprehensive GLP-compliant study plan tailored to your specific method and analyte.
- Rigorous quality control procedures and documentation to ensure the integrity of data and results.
- Expert interpretation and reporting of validation data, providing clear insights into method performance and limitations.
- A GLP-compliant study report that meets regulatory requirements and supports regulatory submissions.
