Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm
Editat de Ajit S. Narang, Sherif I.F. Badawyen Limba Engleză Hardback – 4 dec 2018
- Discusses fundamentals of theory and current industrial practice in the field of wet granulation, including product and process design and role of material properties in wet granulation
- Examines the modern evolution of wet granulation through current topics such as established and novel process analytical technologies (PATs), and product development and scale-up paradigms
- Written for scientists working within the pharmaceutical industry, as well as academics, regulatory officials and equipment vendors who provide PAT tools and granulation equipment
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Specificații
ISBN-13: 9780128104606
ISBN-10: 0128104600
Pagini: 890
Ilustrații: 40 illustrations (40 in full color)
Dimensiuni: 191 x 235 x 51 mm
Greutate: 1.84 kg
Editura: ELSEVIER SCIENCE
ISBN-10: 0128104600
Pagini: 890
Ilustrații: 40 illustrations (40 in full color)
Dimensiuni: 191 x 235 x 51 mm
Greutate: 1.84 kg
Editura: ELSEVIER SCIENCE
Public țintă
Corporate industry researchers at pharmaceutical, biotechnology, excipient and drug delivery companies, academic researchers and graduate students in the pharmaceutical sciences, equipment manufacturers and chemical engineersCuprins
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