Ajit S. Narang,
Sherif I.F. Badawy
Handbook of Pharmaceutical Wet Granulation
Theory and Practice in a Quality by Design Paradigm
Gebonden Engels 2018 9780128104606Levertijd ± 9 werkdagen
Gratis verzonden
Samenvatting
Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide spectrum of relevant and contemporary wet granulation topics, techniques and processes. The books' focus on process analytical technology, quality by design principles, granulation equipment, modeling, scale-up, control and real time release makes it a timely and valuable resource for all those involved in pharmaceutical wet granulation.
Specificaties
ISBN13:9780128104606
Taal:Engels
Bindwijze:Gebonden
Aantal pagina's:890
Uitgever:Elsevier Science
Hoofdrubriek:Geneeskunde, Inkoop en logistiek
Lezersrecensies
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Inhoudsopgave
Section I: Physicochemical Principles and Fundamentals of Wet Granulation
Section II: Critical Quality Attributes of Drug Products and Process Design Solutions
Section III: Process-Stability Interactions and Optimization
Section IV: Material Attributes Critical to Wet Granulation Process Performance
Section V: Process Modeling
Section VI: Scale-up
Section VII: Process Development and Process Analytical Technology Applications
Section VIII: Real-Time Release, Real-time Release Testing, and Drug Product Control Strategy Development
Section II: Critical Quality Attributes of Drug Products and Process Design Solutions
Section III: Process-Stability Interactions and Optimization
Section IV: Material Attributes Critical to Wet Granulation Process Performance
Section V: Process Modeling
Section VI: Scale-up
Section VII: Process Development and Process Analytical Technology Applications
Section VIII: Real-Time Release, Real-time Release Testing, and Drug Product Control Strategy Development
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