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Development of a Robust Control Strategy for Fixed-Dose Combination Bilayer Tablets with Integrated Quality by Design, Statistical, and Process Analytical Technology Approach.
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- Pharmaceutics, 2021, v. 13, n. 9, p. 1443, doi. 10.3390/pharmaceutics13091443
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- Article
Process Analytical Technology Tools for Monitoring Pharmaceutical Unit Operations: A Control Strategy for Continuous Process Verification.
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- Pharmaceutics, 2021, v. 13, n. 6, p. 919, doi. 10.3390/pharmaceutics13060919
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- Article
Control Strategy for Process Development of High-Shear Wet Granulation and Roller Compaction to Prepare a Combination Drug Using Integrated Quality by Design.
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- Pharmaceutics, 2021, v. 13, n. 1, p. 80, doi. 10.3390/pharmaceutics13010080
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- Article
Model-Based Scale-up Methodologies for Pharmaceutical Granulation.
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- Pharmaceutics, 2020, v. 12, n. 5, p. 453, doi. 10.3390/pharmaceutics12050453
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- Article
New Preclinical Development of a c-Met Inhibitor and Its Combined Anti-Tumor Effect in c-Met-Amplified NSCLC.
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- Pharmaceutics, 2020, v. 12, n. 2, p. 121, doi. 10.3390/pharmaceutics12020121
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- Article
Development of a Resveratrol Nanosuspension Using the Antisolvent Precipitation Method without Solvent Removal, Based on a Quality by Design (QbD) Approach.
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- Pharmaceutics, 2019, v. 11, n. 12, p. 688, doi. 10.3390/pharmaceutics11120688
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- Article
Application of the Discrete Element Method for Manufacturing Process Simulation in the Pharmaceutical Industry.
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- Pharmaceutics, 2019, v. 11, n. 8, p. 414, doi. 10.3390/pharmaceutics11080414
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- Article
Scale-Up Strategy in Quality by Design Approach for Pharmaceutical Blending Process with Discrete Element Method Simulation.
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- Pharmaceutics, 2019, v. 11, n. 6, p. 264, doi. 10.3390/pharmaceutics11060264
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- Article
Comprehensive Study of Intermediate and Critical Quality Attributes for Process Control of High-Shear Wet Granulation Using Multivariate Analysis and the Quality by Design Approach.
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- Pharmaceutics, 2019, v. 11, n. 6, p. 252, doi. 10.3390/pharmaceutics11060252
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- Article
Pharmacokinetics of eperisone following oral administration in healthy Korean volunteers.
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- Biopharmaceutics & Drug Disposition, 2021, v. 42, n. 2, p. 94, doi. 10.1002/bdd.2264
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- Article
Effects of granulation process variables on the physical properties of dosage forms by combination of experimental design and principal component analysis.
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- Asian Journal of Pharmaceutical Sciences, 2019, v. 14, n. 3, p. 287, doi. 10.1016/j.ajps.2018.08.006
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- Article
Enhanced Oral Bioavailability of Resveratrol by Using Neutralized Eudragit E Solid Dispersion Prepared via Spray Drying.
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- Antioxidants, 2021, v. 10, n. 1, p. 90, doi. 10.3390/antiox10010090
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- Article
Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery.
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- Antioxidants, 2019, v. 8, n. 11, p. 554, doi. 10.3390/antiox8110554
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- Article