@article{3020880,
    title = "Workshop report: USP workshop on advancements in in vitro performance testing of drug products",
    author = "Hermans, A. and Dorozynski, P. and Muzzio, F.J. and Li, H. and Nielsen, S. and Chen, S. and Reppas, C. and Klein, S. and Patel, S. and Wacker, M. and Thakker, K. and Pruessmann, K. and Seidlitz, A. and Ghosh, T.K. and Yang, Y. and Willett, D. and Hochhaus, G. and Tay, J. and Liew, C.V. and Heng, P.W.S. and Sun, C.C. and Kraemer, J. and Marques, M.R.C.",
    journal = "Dissolution Technologies",
    year = "2020",
    volume = "27",
    number = "2",
    pages = "52-70",
    publisher = "Dissolution Technologies Inc",
    doi = "10.14227/DT270220P52",
    keywords = "nanomaterial, Article;  dissolution;  drug delivery system;  drug formulation;  drug granulation;  drug industry;  drug release;  drug solubility;  gastrointestinal transit;  in vitro study;  micro-computed tomography;  microscopy;  mouth cavity;  nuclear magnetic resonance imaging;  product development;  product quality;  quality control;  suppository;  tablet disintegration;  three dimensional printing",
    abstract = "In December 2019, The United States Pharmacopeia (USP) organized a 2-day workshop to explore new approaches to assess in vitro performance of drug products. Experts from around the globe presented processes, techniques, systems that can be used to evaluate and model in vitro performance of different pharmaceutical dosage forms. The following is a summary of most of the presentations and the highlights of the discussions that ensued. © 2020, Dissolution Technologies Inc. All rights reserved."
}