| Effect of Human Error, Inhalation Flow, and Inhalation Volume on Dose Delivery from Ellipta (R) Dry-Powder Inhaler |
9 |
| Hydrogel Containing PEG-Coated Fluconazole Nanoparticles with Enhanced Solubility and Antifungal Activity |
7 |
| Methodology for a Variable Rate Control Strategy Development in Continuous Manufacturing Applied to Twin-screw Wet-Granulation and Continuous Fluid-bed Drying |
7 |
| Formulation and Evaluation of Chitosan-Based Buccal Bioadhesive Films of Zolmitriptan |
6 |
| Mechanochemical Synthesis of Carvedilol Cocrystals Utilizing Hot Melt Extrusion Technology |
6 |
| Methotrexate-Loaded Nanomixed Micelles: Formulation, Characterization, Bioavailability, Safety, and In Vitro Anticancer Study |
6 |
| Subdivision of Tablets Containing Modified Delivery Technology: the Case of Orally Disintegrating Tablets |
6 |
| Optimization of Noscapine-Loaded mPEG-PLGA Nanoparticles and Release Study: a Response Surface Methodology Approach |
6 |
| 5-Fluorocytosine/5-Fluorouracil Drug-Drug Cocrystal: a New Development Route Based on Mechanochemical Synthesis |
5 |
| Residence Time Distribution (RTD)-Based Control System for Continuous Pharmaceutical Manufacturing Process |
5 |
| The Impact of Solid Dispersion on Formulation, Using Confocal Micro Raman Spectroscopy as Tool to Probe Distribution of Components |
4 |
| Response Surface Methodology for Optimization of Ultrasound-Assisted Transdermal Delivery and Skin Retention of Asenapine Maleate |
4 |
| Determining The Pressure-Generating Capacity of The Classical and Alternative In Vitro Dissolution Methods Using a Wireless Motility Capsule |
3 |
| Lamotrigine Lipid Nanoparticles for Effective Treatment of Epilepsy: a Focus on Brain Targeting via Nasal Route |
3 |
| Evaluating the Potential, Applicability, and Effectiveness of Ozone Sterilization Process for Medical Devices |
3 |
| Fractal Aspects of Static and Dynamic Flow Properties of Pharmaceutical Excipients |
3 |
| A Training on: Continuous Manufacturing (Direct Compaction) of Solid Dose Pharmaceutical Products |
3 |
| Analytical Method Development Using Transmission Raman Spectroscopy for Pharmaceutical Assays and Compliance with Regulatory Guidelines-Part I: Transmission Raman Spectroscopy and Method Development |
3 |
| Combined Feedforward/Feedback Control of an Integrated Continuous Granulation Process |
2 |
| Performance Survey and Comparison Between Rapid Sterility Testing Method and Pharmacopoeia Sterility Test |
2 |
| Transdermal Delivery of Ibuprofen Utilizing a Novel Solvent-Free Pressure-sensitive Adhesive (PSA): TEPIA (R) Technology |
2 |
| Compatibility of Polyvinyl Chloride (PVC) Medical Devices and Other Polymeric Materials with Reactive Ion Etching (RIE) and Inductively Couple Plasma (ICP) Sterilization Using a Quality by Design (QbD) Approach |
2 |
| Establishing Patient Centric Specifications for Drug Substance and Drug Product Impurities |
2 |
| Ionic Liquid Forms of Carvedilol: Preparation, Characterization, and Solubility Studies |
2 |
| A Quantitative Disintegration Method for Polymeric Films |
2 |
| Application of Lipid Blend-Based Nanoparticulate Scaffold for Oral Delivery of Antihypertensive Drug: Implication on Process Variables and In Vivo Absorption Assessment |
2 |
| A Review on Solubility Enhancement of Carvedilol-a BCS Class II Drug |
2 |
| Development of Chitosan and Alginate Nanocapsules to Increase the Solubility, Permeability and Stability of Curcumin |
2 |
| Evaluation of an Amplified ATP Bioluminescence Method for Rapid Sterility Testing of Large Volume Parenteral |
2 |
| Enhanced Approaches to the Identification, Evaluation, and Control of Impurities |
2 |
| Neural Network to Understand Process Capability and Process Intermediates Acceptance Criteria in Monoclonal Antibody Production Process |
1 |
| Part 3: Enhanced Approaches to the Development of the Control Strategy and its Implementation in the Manufacturing Process Description |
1 |
| Deriving and Assessing Strategic Priorities for Outsourcing Partner Selection in Pharmaceutical R&D: an Approach Using Analytic Hierarchy Process (AHP) Based on 34 Experts' Responses From Korean Pharmaceutical Industry |
1 |
| Improve Solubility of Acetamidophenol from PEG and Witepsol Suppositories via Formation of Inclusion Complex by beta-Cyclodextrin with a Controlled Release Profile |
1 |
| Advances in Continuous Active Pharmaceutical Ingredient (API) Manufacturing: Real-time Monitoring Using Multivariate Tools |
1 |
| Fractal Aggregation of Dihydroquercetin After Lyophilization |
1 |
| Quantitative Simulation on Powder Shear Flow Using Discrete Element Method |
1 |
| Steady-State Data Reconciliation Framework for a Direct Continuous Tableting Line |
1 |
| D-Optimal Optimization and Data-Analysis Comparison Between a DoE Software and Artificial Neural Networks of a Chitosan Coating Process onto PLGA Nanoparticles for Lung and Cervical Cancer Treatment |
1 |
| Evaluation of a Dry Coating Technology as a Substitute for Roller Compaction for Dry Agglomeration Applications in the Pharmaceutical Industry |
0 |
| Analytical Method Development Using Transmission Raman Spectroscopy for Pharmaceutical Assays and Compliance with Regulatory Guidelines-Part II: Practical Implementation Considerations |
0 |
| Characterization of Self-Emulsifying Drug Delivery Systems Using In Situ Raman Spectroscopy to Study the Precipitation Inhibition Mechanism of Poorly Water-Soluble Drugs |
0 |
| Estimating Number of PPQ Batches: Various Approaches |
0 |
| The Delivery of Flexibility from the Application of QbD to API Development |
0 |
| HPMC-Eudragit-Based Gastro-retentive Hydrodynamically Balanced SystemSuitable for Sparingly Soluble and Freely Soluble Drugs: an In Vitro Study |
0 |
| Development and Robustness Verification of an At-Line Transmission Raman Method for Pharmaceutical Tablets Using Quality by Design (QbD) Principles |
0 |
| Pharmaceutical Start-ups' Technology and Financing Strategy |
0 |
| A System for Real-Time Syringe Classification and Volume Measurement Using a Combination of Image Processing and Artificial Neural Networks |
0 |
| Quality Deviation Handling on the Polymeric Coating of Pharmaceutical Tablets |
0 |
| The Assessment of pH-Induced Supersaturation and Impact of an Additional Drug on the Solution Phase Behavior of Saquinavir |
0 |
