LCMS Method Validation
Intertek provides a team of experienced validation scientists committed to the proper conduct and reporting of validations and related stability assessments according to all internal and client SOPs.
Intertek Alta conducts a thorough method pre-qualification prior to validation, in order to assess the method for precision and accuracy, matrix effects and assay ruggedness. A detailed validation plan is submitted to the client for approval prior to the commencement of work. Senior laboratory staff then conduct a rigorous scientific review to ensure that all validations are scientifically sound, and that they meet or exceed the requirements outlined in the FDA's "Guidance for Industry, Bioanalytical Method Validations" issued in May, 2001.
Related Method Validation Services
Request more information to see how Intertek can help your organization with LCMS Method Validation.