M. Whitmire

A Global GLP Approach to Formulation Analysis Method Validation andSample Analysis

Rebecca Ross, M. Whitmire, Joy Mwalimu, 2015 .

NonClinical Dose Formulation Analysis Method Validation and Sample Analysis

Teresa R. Henry, S. Ohorodnik, P. Bryan, 2010, The AAPS Journal.

Comparison of bioequivalence study regulatory requirements for human and veterinary drugs.

T. Grabowski, J. Jaroszewski, M. Whitmire, 2012, Regulatory toxicology and pharmacology : RTP.

LC-MS/MS Bioanalysis Method Development, Validation, and Sample Analysis: Points to Consider When Conducting Nonclinical and Clinical Studies in Accordance with Current Regulatory Guidances

Monica Whitmire, Jennifer Ammerman, Patricia de Lisio, 2011 .

Technical aspects of inductively coupled plasma bioanalysis techniques.

J. Wieling, J. Sailstad, Phillip Wang, 2013, Bioanalysis.

Nonclinical Dose Formulation: Out of Specification Investigations

Teresa R. Henry, Natalie L. South, S. Ohorodnik, 2012, The AAPS Journal.

Technical aspects of inductively coupled plasma bioanalysis techniques.

J. Wieling, J. Sailstad, Phillip Wang, 2013, Bioanalysis.

An immunoligand assay for quantitation of process specific Escherichia coli host cell contaminant proteins in a recombinant bovine somatotropin.

L. Eaton, M. Whitmire, 1997, Journal of immunoassay.