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Journal of Pharmaceutical Sciences, ISSN 0022-3549, 03/2015, Volume 104, Issue 3, pp. 832 - 839
This white paper provides a perspective of the challenges, research needs, and future directions for control systems engineering in continuous pharmaceutical... 
process analytical technology | dynamic simulation | control systems | mathematical model | manufacturing | quality by design | processing | systems integration | analysis | multivariate analysis | Process analytical technology | Quality by design | Analysis | Control systems | Dynamic simulation | Manufacturing | Mathematical model | Multivariate analysis | Systems integration | Processing | DESIGN | CHEMISTRY, MEDICINAL | CHEMISTRY, MULTIDISCIPLINARY | PHARMACOLOGY & PHARMACY | TECHNOLOGY | Drug Costs | Multivariate Analysis | Drug Industry - trends | Humans | Pharmaceutical Preparations - chemical synthesis | Biomedical Engineering - trends | Public-Private Sector Partnerships | Technology, Pharmaceutical - trends | Drug Industry - methods | Drug Industry - economics | Drug Industry - standards | Quality Control | Pharmaceutical Preparations - economics | Pharmaceutical Preparations - standards | Technology, Pharmaceutical - standards | Technology, Pharmaceutical - economics | Systems Integration | Cooperative Behavior | Technology, Pharmaceutical - methods | Workflow | Forecasting | Molecular Dynamics Simulation | Interdisciplinary Communication | Algorithms | Numerical Analysis, Computer-Assisted | Cost-Benefit Analysis | Biomedical Engineering - standards | Diffusion of Innovation | Biomedical Engineering - methods
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2008, Volume 358, Issue 23, pp. 2457 - 2467
Journal Article
Journal Article
Journal of Pharmaceutical Sciences, ISSN 0022-3549, 03/2015, Volume 104, Issue 3, pp. 803 - 812
This paper assesses the current regulatory environment, relevant regulations and guidelines, and their impact on continuous manufacturing. It summarizes... 
regulatory considerations | control strategy | processing | continuous manufacturing | GMP | validation | unit operations | stability | bioequivalence | ICH | Validation | Unit operations | Stability | Bioequivalence | Continuous manufacturing | Regulatory considerations | Control strategy | Processing | CHEMISTRY, MEDICINAL | CHEMISTRY, MULTIDISCIPLINARY | PHARMACOLOGY & PHARMACY | Guidelines as Topic | Drug Industry - trends | United States | Drug Industry - legislation & jurisprudence | Humans | Drug Industry - instrumentation | Drug Contamination - prevention & control | Pharmaceutical Preparations - chemical synthesis | Technology, Pharmaceutical - trends | Drug Industry - methods | Patient Safety | Drug Contamination - legislation & jurisprudence | Drug Industry - standards | United States Food and Drug Administration | Quality Control | Legislation, Drug - trends | Equipment Contamination - prevention & control | Pharmaceutical Preparations - standards | Technology, Pharmaceutical - legislation & jurisprudence | Technology, Pharmaceutical - standards | Consumer Product Safety | Europe | Technology, Pharmaceutical - methods | Workflow | Technology, Pharmaceutical - instrumentation | Equipment Contamination - legislation & jurisprudence | Equipment Failure | Conferences, meetings and seminars | Conferences and conventions
Journal Article
Chinese Journal of Chemical Engineering, ISSN 1004-9541, 01/2019, Volume 27, Issue 1, pp. 110 - 129
In the present work, the response surface method software was used with five measurement levels with three factors. These were applied for the optimization of... 
Analysis of variance (ANOVA) | Optimum conditions | Response surface method (RSM) | Mixed matrix membranes | ENGINEERING, CHEMICAL | POLYDIMETHYLSILOXANE | DESIGN | NANOCOMPOSITE MEMBRANES | SILICA | PERMEATION PROPERTIES
Journal Article
Journal of Pharmaceutical Sciences, ISSN 0022-3549, 11/2019, Volume 108, Issue 11, pp. 3521 - 3523
We make the case for why continuous pharmaceutical manufacturing is essential, what the barriers are, and how to overcome them. To overcome them, government... 
PAT | advanced manufacturing | regulatory incentives | stockpiles | tax incentives | continuous manufacturing | model-based control | stock-outs | personalized medicine | quality | CHEMISTRY, MEDICINAL | CHEMISTRY, MULTIDISCIPLINARY | PHARMACOLOGY & PHARMACY
Journal Article
Journal of Pharmaceutical Sciences, ISSN 0022-3549, 11/2017, Volume 106, Issue 11, pp. 3199 - 3206
Journal Article
Journal Article
Journal of Pharmaceutical and Biomedical Analysis, ISSN 0731-7085, 2011, Volume 54, Issue 5, pp. 1020 - 1029
Heparin is a naturally produced, heterogeneous compound consisting of variably sulfated and acetylated repeating disaccharide units. The structural complexity... 
Principal components analysis | Heparin | Pattern recognition | Linear discriminant analysis | Proton nuclear magnetic resonance spectroscopy
Journal Article
Analytical Chemistry, ISSN 0003-2700, 02/2011, Volume 83, Issue 3, pp. 1030 - 1039
To differentiate heparin samples with varying amounts of dermatan sulfate (DS) impurities and oversulfated chondroitin sulfate (OSCS) contaminants, proton NMR... 
Protons | Pharmaceutical Preparations - analysis | Magnetic Resonance Spectroscopy - methods
Journal Article
Analytical Chemistry, ISSN 0003-2700, 12/2010, Volume 82, Issue 23, p. 9865
Here we report results from the analyses by enzymatic digestion and reversed-phase ion-pairing liquid chromatography mass spectrometry (RPIP-LC-MS) of active... 
Analytical chemistry | Drugs | Enzymes | Ion chromatography | Mass spectrometry
Journal Article
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