Method Development & Validation
Azopharma offers method development and validation of bioanalytical methods in a wide variety of biological matrices utilizing solid-phase extraction (SPE) and solvent extraction with LC/MS/MS, HPLC and GC quantitation, as appropriate.
When method development or modification is necessary, we will review information provided by you or from a literature search. A method will then be developed based on that information as well as our extensive experience. All methods are validated to document the performance of the method in our laboratory before conducting sample analyses. Method validation is conducted under GLP regulations according to industry/FDA criteria, unless requested otherwise.
In addition, we can also transfer in your existing proprietary validated methods.