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Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
by
Yu, Lawrence X.
in
Administration, Oral
/ Biochemistry
/ Biological and medical sciences
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Chemistry, Pharmaceutical - standards
/ Consumer Product Safety
/ Dosage Forms
/ Drug Compounding - standards
/ Drug Contamination - prevention & control
/ Drugs, Generic - administration & dosage
/ Drugs, Generic - chemistry
/ Drugs, Generic - standards
/ General pharmacology
/ Guidelines as Topic
/ Humans
/ Medical Law
/ Medical sciences
/ Pharmaceutical industry
/ Pharmaceutical technology. Pharmaceutical industry
/ Pharmacology. Drug treatments
/ Pharmacology/Toxicology
/ Pharmacy
/ Prescription drugs
/ Process controls
/ Product quality
/ Production controls
/ Quality Control
/ Research Paper
/ Technology, Pharmaceutical - standards
2008
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Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
by
Yu, Lawrence X.
in
Administration, Oral
/ Biochemistry
/ Biological and medical sciences
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Chemistry, Pharmaceutical - standards
/ Consumer Product Safety
/ Dosage Forms
/ Drug Compounding - standards
/ Drug Contamination - prevention & control
/ Drugs, Generic - administration & dosage
/ Drugs, Generic - chemistry
/ Drugs, Generic - standards
/ General pharmacology
/ Guidelines as Topic
/ Humans
/ Medical Law
/ Medical sciences
/ Pharmaceutical industry
/ Pharmaceutical technology. Pharmaceutical industry
/ Pharmacology. Drug treatments
/ Pharmacology/Toxicology
/ Pharmacy
/ Prescription drugs
/ Process controls
/ Product quality
/ Production controls
/ Quality Control
/ Research Paper
/ Technology, Pharmaceutical - standards
2008
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Do you wish to request the book?
Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
by
Yu, Lawrence X.
in
Administration, Oral
/ Biochemistry
/ Biological and medical sciences
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Biomedicine
/ Chemistry, Pharmaceutical - standards
/ Consumer Product Safety
/ Dosage Forms
/ Drug Compounding - standards
/ Drug Contamination - prevention & control
/ Drugs, Generic - administration & dosage
/ Drugs, Generic - chemistry
/ Drugs, Generic - standards
/ General pharmacology
/ Guidelines as Topic
/ Humans
/ Medical Law
/ Medical sciences
/ Pharmaceutical industry
/ Pharmaceutical technology. Pharmaceutical industry
/ Pharmacology. Drug treatments
/ Pharmacology/Toxicology
/ Pharmacy
/ Prescription drugs
/ Process controls
/ Product quality
/ Production controls
/ Quality Control
/ Research Paper
/ Technology, Pharmaceutical - standards
2008
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Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
Journal Article
Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control
2008
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Overview
Purpose
The purpose of this paper is to discuss the pharmaceutical Quality by Design (QbD) and describe how it can be used to ensure pharmaceutical quality.
Materials and Methods
The QbD was described and some of its elements identified. Process parameters and quality attributes were identified for each unit operation during manufacture of solid oral dosage forms. The use of QbD was contrasted with the evaluation of product quality by testing alone.
Results
The QbD is a systemic approach to pharmaceutical development. It means designing and developing formulations and manufacturing processes to ensure predefined product quality. Some of the QbD elements include:
Defining target product quality profile
Designing product and manufacturing processes
Identifying critical quality attributes, process parameters, and sources of variability
Controlling manufacturing processes to produce consistent quality over time
Conclusions
Using QbD, pharmaceutical quality is assured by understanding and controlling formulation and manufacturing variables. Product testing confirms the product quality. Implementation of QbD will enable transformation of the chemistry, manufacturing, and controls (CMC) review of abbreviated new drug applications (ANDAs) into a science-based pharmaceutical quality assessment.
Publisher
Springer US,Springer,Springer Nature B.V
Subject
/ Biological and medical sciences
/ Biomedical and Life Sciences
/ Biomedical Engineering and Bioengineering
/ Chemistry, Pharmaceutical - standards
/ Drug Compounding - standards
/ Drug Contamination - prevention & control
/ Drugs, Generic - administration & dosage
/ Humans
/ Pharmaceutical technology. Pharmaceutical industry
/ Pharmacology. Drug treatments
/ Pharmacy
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