Mark R Berry

Statistical assessment of dissolution and drug release profile similarity using a model-dependent approach.

Mark R Berry, Michael D Likar, M. D. Likar, 2007, Journal of pharmaceutical and biomedical analysis.

Probability of passing dissolution acceptance criteria for an immediate release tablet.

B. Nickerson, M. Dumont, Mark R Berry, 2007, Journal of pharmaceutical and biomedical analysis.

Leveraging elevated temperature and particle size reduction to extract API from various tablet formulations.

B. Nickerson, Mark R Berry, Tim L. Houck, 2008, Journal of pharmaceutical and biomedical analysis.

Validation of a dissolution method with HPLC analysis for lasofoxifene tartrate low dose tablets.

B. Nickerson, M. Dumont, Mark R Berry, 2007, Journal of pharmaceutical and biomedical analysis.

Investigation of Design Space for Freeze-Drying: Use of Modeling for Primary Drying Segment of a Freeze-Drying Cycle

Sumit Luthra, Liling Zhang, Venkat Rao Koganti, 2011, AAPS PharmSciTech.

Application of Modeling to Scale-up Dissolution in Pharmaceutical Manufacturing

Y. Waghmare, Rick Falk, V. Koganti, 2010, AAPS PharmSciTech.