Bioanalytical Services
Method Development, Validation & Transfer
Cyanta 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.
Our scientists are experts in method development and pride themselves on creating a method that is applicable to your molecule: small or large. Coming at the development from all angles we aim to generate a specific, selective, robust method that can move from discovery to development.
All methods are validated or transferred to document the performance of the method in our laboratory before conducting sample analyses. Method validations and method transfers are conducted under GLP regulations according to industry/FDA criteria, unless requested otherwise.
When method development or modification is necessary, Cyanta will review information provided by you or from a literature search. We will then develop a method based on that information as well as our extensive experience.