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Book Synopsis The Control of Raw Materials by : Joel Hurstfield
Download or read book The Control of Raw Materials written by Joel Hurstfield and published by Krause Publications. This book was released on 1953 with total page 554 pages. Available in PDF, EPUB and Kindle. Book excerpt:
This book, first published in 1936, addresses the need for a comprehensive study of the development of international control in the field of certain vital commodities and services. It traces tendencies of development in government policy, and shows the growth of governmental or semi-governmental machinery of an international kind, that aims at regulating the production and distribution of raw materials, foodstuffs and services.
Book Synopsis Raw Materials and International Control by : H.R.G. Greaves
Download or read book Raw Materials and International Control written by H.R.G. Greaves and published by Routledge. This book was released on 2017-10-10 with total page 172 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book, first published in 1936, addresses the need for a comprehensive study of the development of international control in the field of certain vital commodities and services. It traces tendencies of development in government policy, and shows the growth of governmental or semi-governmental machinery of an international kind, that aims at regulating the production and distribution of raw materials, foodstuffs and services.
Book Synopsis The Control of Raw Materials by : Joel Hurstfield
Download or read book The Control of Raw Materials written by Joel Hurstfield and published by . This book was released on 1984 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis The Control of Raw Materials by : Joel Hurstfield
Download or read book The Control of Raw Materials written by Joel Hurstfield and published by . This book was released on 1953 with total page 200 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Now in one volume-all the raw materials used in the ceramic and glass industries A basic understanding of where raw materials come from and how they are processed is critical to attaining consistent raw material batches-an essential factor to maintaining steady production. The solution is Raw Materials for Glass and Ceramics, a complete resource of up-to-date information and analysis on the raw materials used in the glass and ceramic industries. Raw Materials for Glass and Ceramics presents all classes of materials, the roles they play, their sources and extraction processes, and quality control issues and regulations impacting the industry, as well as: A thorough description of the formation and evaluation of raw material deposits and location of the important sources Complete analysis of all the raw materials used in the ceramic and glass industries, including natural, processed, recycled, and synthetic materials An explanation of the raw materials industry, including transportation, environmental and health concerns, and quality specifications
Book Synopsis Raw Materials for Glass and Ceramics by : Christopher W. Sinton
Download or read book Raw Materials for Glass and Ceramics written by Christopher W. Sinton and published by John Wiley & Sons. This book was released on 2006-03-17 with total page 376 pages. Available in PDF, EPUB and Kindle. Book excerpt: Now in one volume-all the raw materials used in the ceramic and glass industries A basic understanding of where raw materials come from and how they are processed is critical to attaining consistent raw material batches-an essential factor to maintaining steady production. The solution is Raw Materials for Glass and Ceramics, a complete resource of up-to-date information and analysis on the raw materials used in the glass and ceramic industries. Raw Materials for Glass and Ceramics presents all classes of materials, the roles they play, their sources and extraction processes, and quality control issues and regulations impacting the industry, as well as: A thorough description of the formation and evaluation of raw material deposits and location of the important sources Complete analysis of all the raw materials used in the ceramic and glass industries, including natural, processed, recycled, and synthetic materials An explanation of the raw materials industry, including transportation, environmental and health concerns, and quality specifications
This volume in the AAPS Advances series covers various quality, safety and clinical aspects of drug development that are relevant to new and/or generic drugs containing a complex mixture of molecules. Specific topics discussed include: raw materials sourcing; manufacturing controls; characterization; identification of critical product quality components and attributes; identification of impurities, particularly as they bear on toxicity and immunogenicity; clinical trial study design considerations, and the regulatory science applications to development of such complex mixtures. Complex mixtures are challenging to characterize and analyze using standard methods. Further challenges extend throughout the product development cycle from raw material control to clinical study design. The regulatory landscape is rapidly changing as new types of complex mixtures are introduced into clinical trials and to the market (e.g., traditional Chinese medicines and medical marijuana products), while older products are facing generic competition for the first time (e.g., enoxaparin). The future outlook for complex generic drug products, as opposed to the more commonly developed targeted single agent drug products is not clear. The risks pertaining to lack of a full understanding of raw material control, process and controls in manufacture, as well as characterization of a complex mixture were seen vividly during the heparin crisis of 2008. As such powerful lessons have been learned about the regulatory science specific to complex products. The Science and Regulations of Naturally Derived Complex Drugs addresses the interests among industry, academics, and government on the issues surrounding the future development of mixtures for medicinal use.
Book Synopsis The Science and Regulations of Naturally Derived Complex Drugs by : Ram Sasisekharan
Download or read book The Science and Regulations of Naturally Derived Complex Drugs written by Ram Sasisekharan and published by Springer. This book was released on 2019-04-23 with total page 331 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume in the AAPS Advances series covers various quality, safety and clinical aspects of drug development that are relevant to new and/or generic drugs containing a complex mixture of molecules. Specific topics discussed include: raw materials sourcing; manufacturing controls; characterization; identification of critical product quality components and attributes; identification of impurities, particularly as they bear on toxicity and immunogenicity; clinical trial study design considerations, and the regulatory science applications to development of such complex mixtures. Complex mixtures are challenging to characterize and analyze using standard methods. Further challenges extend throughout the product development cycle from raw material control to clinical study design. The regulatory landscape is rapidly changing as new types of complex mixtures are introduced into clinical trials and to the market (e.g., traditional Chinese medicines and medical marijuana products), while older products are facing generic competition for the first time (e.g., enoxaparin). The future outlook for complex generic drug products, as opposed to the more commonly developed targeted single agent drug products is not clear. The risks pertaining to lack of a full understanding of raw material control, process and controls in manufacture, as well as characterization of a complex mixture were seen vividly during the heparin crisis of 2008. As such powerful lessons have been learned about the regulatory science specific to complex products. The Science and Regulations of Naturally Derived Complex Drugs addresses the interests among industry, academics, and government on the issues surrounding the future development of mixtures for medicinal use.
Book Synopsis International Control of Raw Materials by : Benjamin Bruce Wallace
Download or read book International Control of Raw Materials written by Benjamin Bruce Wallace and published by . This book was released on 1983 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Foreign Combinations to Control Prices of Raw Materials by : United States. Dept. of Commerce
Download or read book Foreign Combinations to Control Prices of Raw Materials written by United States. Dept. of Commerce and published by . This book was released on 1926 with total page 36 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Raw Materials and International Control by : Harold Richard Goring Greaves
Download or read book Raw Materials and International Control written by Harold Richard Goring Greaves and published by . This book was released on 1936 with total page 166 pages. Available in PDF, EPUB and Kindle. Book excerpt:
The concepts, applications, and practical issues of Quality by Design Quality by Design (QbD) is a new framework currently being implemented by the FDA, as well as EU and Japanese regulatory agencies, to ensure better understanding of the process so as to yield a consistent and high-quality pharmaceutical product. QbD breaks from past approaches in assuming that drug quality cannot be tested into products; rather, it must be built into every step of the product creation process. Quality by Design: Perspectives and Case Studies presents the first systematic approach to QbD in the biotech industry. A comprehensive resource, it combines an in-depth explanation of basic concepts with real-life case studies that illustrate the practical aspects of QbD implementation. In this single source, leading authorities from the biotechnology industry and the FDA discuss such topics as: The understanding and development of the product's critical quality attributes (CQA) Development of the design space for a manufacturing process How to employ QbD to design a formulation process Raw material analysis and control strategy for QbD Process Analytical Technology (PAT) and how it relates to QbD Relevant PAT tools and applications for the pharmaceutical industry The uses of risk assessment and management in QbD Filing QbD information in regulatory documents The application of multivariate data analysis (MVDA) to QbD Filled with vivid case studies that illustrate QbD at work in companies today, Quality by Design is a core reference for scientists in the biopharmaceutical industry, regulatory agencies, and students.
Book Synopsis Quality by Design for Biopharmaceuticals by : Anurag S. Rathore
Download or read book Quality by Design for Biopharmaceuticals written by Anurag S. Rathore and published by John Wiley & Sons. This book was released on 2011-09-20 with total page 279 pages. Available in PDF, EPUB and Kindle. Book excerpt: The concepts, applications, and practical issues of Quality by Design Quality by Design (QbD) is a new framework currently being implemented by the FDA, as well as EU and Japanese regulatory agencies, to ensure better understanding of the process so as to yield a consistent and high-quality pharmaceutical product. QbD breaks from past approaches in assuming that drug quality cannot be tested into products; rather, it must be built into every step of the product creation process. Quality by Design: Perspectives and Case Studies presents the first systematic approach to QbD in the biotech industry. A comprehensive resource, it combines an in-depth explanation of basic concepts with real-life case studies that illustrate the practical aspects of QbD implementation. In this single source, leading authorities from the biotechnology industry and the FDA discuss such topics as: The understanding and development of the product's critical quality attributes (CQA) Development of the design space for a manufacturing process How to employ QbD to design a formulation process Raw material analysis and control strategy for QbD Process Analytical Technology (PAT) and how it relates to QbD Relevant PAT tools and applications for the pharmaceutical industry The uses of risk assessment and management in QbD Filing QbD information in regulatory documents The application of multivariate data analysis (MVDA) to QbD Filled with vivid case studies that illustrate QbD at work in companies today, Quality by Design is a core reference for scientists in the biopharmaceutical industry, regulatory agencies, and students.