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Pharmaceutical Development and Technology|September 24, 2009
Comparative evaluation of the powder and compression properties of various grades and brands of microcrystalline cellulose by multivariate methodsRahul V Haware, Annette Bauer-Brandl, Ingunn ThoEuropean Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|December 17, 2008
Application of multivariate methods to compression behavior evaluation of directly compressible materialsRahul V Haware, Ingunn Tho, Annette Bauer-BrandlEuropean Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|August 25, 2009
Multivariate analysis of relationships between material properties, process parameters and tablet tensile strength for alpha-lactose monohydratesRahul V Haware, Ingunn Tho, Annette Bauer-BrandlExpert Opinion on Drug Delivery|November 22, 2011
Quality by design (QbD) approaches for the compression step of tabletingIngunn Tho, Annette Bauer-BrandlAAPS Pharmscitech|December 17, 2009
Direct compression behavior of low- and high-methoxylated pectinsLinda Salbu, Annette Bauer-Brandl, Ingunn ThoPharmaceutical Development and Technology|December 15, 2010
Effect of degree of methoxylation and particle size on compression properties and compactibility of pectin powdersLinda Salbu, Annette Bauer-Brandl, Göran Alderborn, et al.European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|December 4, 2018
Oromucosal drug delivery: Trends in in-vitro biopharmaceutical assessment of new chemical entities and formulationsMartin Brandl, Annette Bauer-BrandlInternational Journal of Pharmaceutics|April 25, 2003
Note on the measurement of flowability according to the European PharmacopoeiaAndrea Schüssele, Annette Bauer-BrandlTidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 23, 2012
[Orally disintegrating tablets--advantages and drawbacks]Ingunn ThoPharmaceutical Research|April 3, 2003
Thermodynamics of solutions I: benzoic acid and acetylsalicylic acid as models for drug substances and the prediction of solubilityGerman L Perlovichl, Annette Bauer-BrandlPageof 21