Simon Curtis

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formulation drug delivery oral drug delivery drug design drug controlled release solid form parenteral transdermal hot melt extrusion nano particle biotech pharmaceutical preclinical modified nanosuspension bioavailability amorphous solubility ocular biotechnology pharma stability synchrotron reputation crisis pr public relations analytical permeable regulatory soluble supersaturation cro ivivc ba/be pkpd generic clinical development bioequivalence biosimilar biowaver development formulation screening cocrystal

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Solubilities of Crystalline Drugs in Polymers: An Improved Analytical Method and Comparison of Solubilities of Indomethacin and Nifedipine in PVP, PVP/VA, and PVAc

Vor 11 Jahren • 1340 Aufrufe

Simon Curtis

Präsentationen

Amorphous Solid Dispersions: Application Of Spray Drying Formulations For Discovery Toxicology Studies

Nanosuspension – An unique tool for improving the bioavailability of poorly soluble drugs

Bioavailability solubility conference 2011

Pharmaceutical Solid Form

Solubility boston-2012-published

Expediting Time-to-Market and Reducing Time-to-Launch with Physicochemical Optimization

Pharmaceutical Solid Form

Applications of Modified Release during the Preclinical Stage - Weijia Zheng, AstraZeneca

Decreasing Time-to-Market via Synchrotron Utilization to Discover Stable Formulation

Dokumente

Cocrystal review 2011

Solubilities of Crystalline Drugs in Polymers: An Improved Analytical Method and Comparison of Solubilities of Indomethacin and Nifedipine in PVP, PVP/VA, and PVAc

The A to Z of pharmaceutical cocrystals: a decade of fast-moving new science and patents

Oral Drug Formulation Innovations 2014

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