Pharmaceutical Quality by Design

Pharmaceutical Quality by Design
Author: Walkiria S. Schlindwein,Mark Gibson
Publsiher: John Wiley & Sons
Total Pages: 368
Release: 2018-01-05
ISBN 10: 1118895215
ISBN 13: 9781118895214
Language: EN, FR, DE, ES & NL

Pharmaceutical Quality by Design Book Review:

A practical guide to Quality by Design for pharmaceutical product development Pharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative approach is based on the application of product and process understanding underpinned by a systematic methodology which can enable pharmaceutical companies to ensure that quality is built into the product. Familiarity with Quality by Design is essential for scientists working in the pharmaceutical industry. The authors take a practical approach and put the focus on the industrial aspects of the new QbD approach to pharmaceutical product development and manufacturing. The text covers quality risk management tools and analysis, applications of QbD to analytical methods, regulatory aspects, quality systems and knowledge management. In addition, the book explores the development and manufacture of drug substance and product, design of experiments, the role of excipients, multivariate analysis, and include several examples of applications of QbD in actual practice. This important resource: Covers the essential information about Quality by Design (QbD) that is at the heart of modern pharmaceutical development Puts the focus on the industrial aspects of the new QbD approach Includes several illustrative examples of applications of QbD in practice Offers advanced specialist topics that can be systematically applied to industry Pharmaceutical Quality by Design offers a guide to the principles and application of Quality by Design (QbD), the holistic approach to manufacturing that offers a complete understanding of the manufacturing processes involved, in order to yield consistent and high quality products.

Pharmaceutical Quality by Design

Pharmaceutical Quality by Design
Author: Sarwar Beg,Md Saquib Hasnain
Publsiher: Academic Press
Total Pages: 448
Release: 2019-03-27
ISBN 10: 0128163720
ISBN 13: 9780128163726
Language: EN, FR, DE, ES & NL

Pharmaceutical Quality by Design Book Review:

Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to patients. The book walks readers through the QbD framework by covering the fundamental principles of QbD, the current regulatory requirements, and the applications of QbD at various stages of pharmaceutical product development, including drug substance and excipient development, analytical development, formulation development, dissolution testing, manufacturing, stability studies, bioequivalence testing, risk and assessment, and clinical trials. Contributions from global leaders in QbD provide specific insight in its application in a diversity of pharmaceutical products, including nanopharmaceuticals, biopharmaceuticals, and vaccines. The inclusion of illustrations, practical examples, and case studies makes this book a useful reference guide to pharmaceutical scientists and researchers who are engaged in the formulation of various delivery systems and the analysis of pharmaceutical product development and drug manufacturing process. Discusses vital QbD precepts and fundamental aspects of QbD implementation in the pharma, biopharma and biotechnology industries Provides helpful illustrations, practical examples and research case studies to explain QbD concepts to readers Includes contributions from global leaders and experts from academia, industry and regulatory agencies

Quality by Design for Biopharmaceutical Drug Product Development

Quality by Design for Biopharmaceutical Drug Product Development
Author: Feroz Jameel,Susan Hershenson,Mansoor A. Khan,Sheryl Martin-Moe
Publsiher: Springer
Total Pages: 710
Release: 2015-04-01
ISBN 10: 1493923161
ISBN 13: 9781493923168
Language: EN, FR, DE, ES & NL

Quality by Design for Biopharmaceutical Drug Product Development Book Review:

This volume explores the application of Quality by Design (QbD) to biopharmaceutical drug product development. Twenty-eight comprehensive chapters cover dosage forms, liquid and lyophilized drug products. The introductory chapters of this book define key elements of QbD and examine how these elements are integrated into drug product development. These chapters also discuss lessons learned from the FDA Office of Biotechnology Products pilot program. Following chapters demonstrate how QbD is used for formulation development ranging from screening of formulations to developability assessment to development of lyophilized and liquid formats. The next few chapters study the use of small-scale and surrogate models as well as QbD application to drug product processes such as drug substance freezing and thawing, mixing, sterile filtration, filling, lyophilization, inspection and shipping and handling. Later chapters describe more specialized applications of QbD in the drug product realm. This includes the use of QbD in primary containers, devices and combination product development. The volume also explores QbD applied to vaccine development, automation, mathematical modeling and monitoring, and controlling processes and defining control strategies. It concludes with a discussion on the application of QbD to drug product technology transfer as well as overall regulatory considerations and lifecycle management. Quality by Design for Biopharmaceutical Drug Product Development is an authoritative resource for scientists and researchers interested in expanding their knowledge on QbD principles and uses in creating better drugs.

The Housing Design Handbook

The Housing Design Handbook
Author: David Levitt
Publsiher: Routledge
Total Pages: 288
Release: 2012-12-06
ISBN 10: 1135871760
ISBN 13: 9781135871765
Language: EN, FR, DE, ES & NL

The Housing Design Handbook Book Review:

How well have architects succeeded in building housing and what lessons can be learned from their triumphs and failures? The Housing Design Handbook will give you a complete understanding of what makes successful housing design. Through the analysis of work by Levitt Bernstein and a wide range of other UK practices, it illustrates good design principles and accumulates a wealth of knowledge in a readily accessible format for the first time. Written by a recognised authority in the field, the book provides: a range of cases to illustrate the way that different issues in the design of housing have been approached and with what degree of success a review of the place of housing as the most significant built form in the urban landscape an understanding of the importance of achieving a sense of place as the bedrock of social continuity a discussion of how flexibility might be achieved in order to accommodate future changes in housing need, if wholesale demolition and replacement is to be avoided more recent examples which explore why certain social groupings are more resistant to design innovation than others and why there has been such an architectural breakthrough in market led, higher density urban living. David Levitt examines the ideas behind the schemes and assesses how successful and sustainable those ideas have proved, making this an essential reference for professionals and students practicing and studying the design and commissioning of housing.

Handbook of Analytical Quality by Design

Handbook of Analytical Quality by Design
Author: Sarwar Beg,Md Saquib Hasnain,Mahfoozur Rahman,Waleed H. Almalki
Publsiher: Academic Press
Total Pages: 222
Release: 2021-01-09
ISBN 10: 0128203331
ISBN 13: 9780128203330
Language: EN, FR, DE, ES & NL

Handbook of Analytical Quality by Design Book Review:

Handbook of Analytical Quality by Design addresses the steps involved in analytical method development and validation in an effort to avoid quality crises in later stages. The AQbD approach significantly enhances method performance and robustness which are crucial during inter-laboratory studies and also affect the analytical lifecycle of the developed method. Sections cover sample preparation problems and the usefulness of the QbD concept involving Quality Risk Management (QRM), Design of Experiments (DoE) and Multivariate (MVT) Statistical Approaches to solve by optimizing the developed method, along with validation for different techniques like HPLC, UPLC, UFLC, LC-MS and electrophoresis. This will be an ideal resource for graduate students and professionals working in the pharmaceutical industry, analytical chemistry, regulatory agencies, and those in related academic fields. Concise language for easy understanding of the novel and holistic concept Covers key aspects of analytical development and validation Provides a robust, flexible, operable range for an analytical method with greater excellence and regulatory compliance

Quality by Design for Biopharmaceuticals

Quality by Design for Biopharmaceuticals
Author: Anurag S. Rathore,Rohin Mhatre
Publsiher: John Wiley & Sons
Total Pages: 312
Release: 2011-09-20
ISBN 10: 1118210913
ISBN 13: 9781118210918
Language: EN, FR, DE, ES & NL

Quality by Design for Biopharmaceuticals Book Review:

The concepts, applications, and practical issues of Quality byDesign Quality by Design (QbD) is a new framework currently beingimplemented by the FDA, as well as EU and Japanese regulatoryagencies, to ensure better understanding of the process so as toyield a consistent and high-quality pharmaceutical product. QbDbreaks from past approaches in assuming that drug quality cannot betested into products; rather, it must be built into every step ofthe product creation process. Quality by Design: Perspectives and Case Studies presentsthe first systematic approach to QbD in the biotech industry. Acomprehensive resource, it combines an in-depth explanation ofbasic concepts with real-life case studies that illustrate thepractical aspects of QbD implementation. In this single source, leading authorities from thebiotechnology industry and the FDA discuss such topics as: The understanding and development of the product's criticalquality attributes (CQA) Development of the design space for a manufacturingprocess 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 toQbD Relevant PAT tools and applications for the pharmaceuticalindustry The uses of risk assessment and management in QbD Filing QbD information in regulatory documents The application of multivariate data analysis (MVDA) toQbD Filled with vivid case studies that illustrate QbD at work incompanies today, Quality by Design is a core reference forscientists in the biopharmaceutical industry, regulatory agencies,and students.

Juran on Quality by Design

Juran on Quality by Design
Author: J. M. Juran
Publsiher: Simon and Schuster
Total Pages: 538
Release: 1992
ISBN 10: 0029166837
ISBN 13: 9780029166833
Language: EN, FR, DE, ES & NL

Juran on Quality by Design Book Review:

Offers practical advice on planning, setting, and achieving quality goals, looks at three case studies, and explains why quality is essential for business success

Quality by Design

Quality by Design
Author: Nicolo Belavendram
Publsiher: Anonim
Total Pages: 544
Release: 1995
ISBN 10:
ISBN 13: UOM:39015032514245
Language: EN, FR, DE, ES & NL

Quality by Design Book Review:

With the intention of making Taguchi techniques more widely understood, this book covers product and process experiments designed to help quality-manufacturing-design engineers make these products and processes more robust.

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture
Author: Gintaras V. Reklaitis,Christine Seymour,Salvador García-Munoz
Publsiher: John Wiley & Sons
Total Pages: 416
Release: 2017-09-01
ISBN 10: 1119356172
ISBN 13: 9781119356172
Language: EN, FR, DE, ES & NL

Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture Book Review:

Covers a widespread view of Quality by Design (QbD) encompassing the many stages involved in the development of a new drug product. The book provides a broad view of Quality by Design (QbD) and shows how QbD concepts and analysis facilitate the development and manufacture of high quality products. QbD is seen as a framework for building process understanding, for implementing robust and effective manufacturing processes and provides the underpinnings for a science-based regulation of the pharmaceutical industry. Edited by the three renowned researchers in the field, Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture guides pharmaceutical engineers and scientists involved in product and process development, as well as teachers, on how to utilize QbD practices and applications effectively while complying with government regulations. The material is divided into three main sections: the first six chapters address the role of key technologies, including process modeling, process analytical technology, automated process control and statistical methodology in supporting QbD and establishing the associated design space. The second section consisting of seven chapters present a range of thoroughly developed case studies in which the tools and methodologies discussed in the first section are used to support specific drug substance and drug-product QbD related developments. The last section discussed the needs for integrated tools and reviews the status of information technology tools available for systematic data and knowledge management to support QbD and related activities. Highlights Demonstrates Quality by Design (QbD) concepts through concrete detailed industrial case studies involving of the use of best practices and assessment of regulatory implications Chapters are devoted to applications of QbD methodology in three main processing sectors—drug substance process development, oral drug product manufacture, parenteral product processing, and solid-liquid processing Reviews the spectrum of process model types and their relevance, the range of state-of-the-art real-time monitoring tools and chemometrics, and alternative automatic process control strategies and methods for both batch and continuous processes The role of the design space is demonstrated through specific examples and the importance of understanding the risk management aspects of design space definition is highlighted Comprehensive Quality by Design for Pharmaceutical Product Development and Manufacture is an ideal book for practitioners, researchers, and graduate students involved in the development, research, or studying of a new drug and its associated manufacturing process.

World Class Quality

World Class Quality
Author: Keki R. Bhote
Publsiher: AMACOM Div American Mgmt Assn
Total Pages: 487
Release: 2000
ISBN 10: 9780814426425
ISBN 13: 0814426425
Language: EN, FR, DE, ES & NL

World Class Quality Book Review:

This revised, expanded best-seller is a powerful new tool kit for the 21st century.

Chemical Engineering in the Pharmaceutical Industry Active Pharmaceutical Ingredients

Chemical Engineering in the Pharmaceutical Industry  Active Pharmaceutical Ingredients
Author: David J. am Ende,Mary T. am Ende
Publsiher: Wiley
Total Pages: 1168
Release: 2019-04-23
ISBN 10: 1119285860
ISBN 13: 9781119285861
Language: EN, FR, DE, ES & NL

Chemical Engineering in the Pharmaceutical Industry Active Pharmaceutical Ingredients Book Review:

A guide to the development and manufacturing of pharmaceutical products written for professionals in the industry, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry is a practical book that highlights chemistry and chemical engineering. The book’s regulatory quality strategies target the development and manufacturing of pharmaceutically active ingredients of pharmaceutical products. The expanded second edition contains revised content with many new case studies and additional example calculations that are of interest to chemical engineers. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API’s) and 2) Drug Product Design, Development and Modeling. The active pharmaceutical ingredients book puts the focus on the chemistry, chemical engineering, and unit operations specific to development and manufacturing of the active ingredients of the pharmaceutical product. The drug substance operations section includes information on chemical reactions, mixing, distillations, extractions, crystallizations, filtration, drying, and wet and dry milling. In addition, the book includes many applications of process modeling and modern software tools that are geared toward batch-scale and continuous drug substance pharmaceutical operations. This updated second edition: • Contains 30new chapters or revised chapters specific to API, covering topics including: manufacturing quality by design, computational approaches, continuous manufacturing, crystallization and final form, process safety • Expanded topics of scale-up, continuous processing, applications of thermodynamics and thermodynamic modeling, filtration and drying • Presents updated and expanded example calculations • Includes contributions from noted experts in the field Written for pharmaceutical engineers, chemical engineers, undergraduate and graduate students, and professionals in the field of pharmaceutical sciences and manufacturing, the second edition of Chemical Engineering in the Pharmaceutical Industry focuses on the development and chemical engineering as well as operations specific to the design, formulation, and manufacture of drug substance and products.

Handbook of Total Quality Management

Handbook of Total Quality Management
Author: Christian N. Madu
Publsiher: Springer Science & Business Media
Total Pages: 801
Release: 2012-12-06
ISBN 10: 1461552818
ISBN 13: 9781461552819
Language: EN, FR, DE, ES & NL

Handbook of Total Quality Management Book Review:

Quality issues are occupying an increasingly prominent position in today's global business market, with firms seeking to compete on an international level on both price and quality. Consumers are demanding higher quality standards from manufacturers and service providers, while virtually all industrialized nations have instituted quality programs to help indigenous corporations. A proliferation in nation-wide and regional quality awards such as the Baldridge award and certification to ISO 9000 series are making corporations world-wide quality-conscious and eager to implement programs of continuous improvement. To achieve competitiveness, quality practice is a necessity and this book offers an exposition of how quality can be attained. The Handbook of Total Quality Management: Explores in separate chapters new topics such as re-engineering, concurrent engineering, ISO standards, QFD, the Internet, the environment, advanced manufacturing technology and benchmarking Discusses the views of leading quality practitioners such as Derning, Juran, Ishikawa, Crosby and Taguchi throughout the book Considers important strategies for quality improvement, including initiation and performance evaluation through auditing, re-engineering, and process and design innovations. With contributions from 47 authors in 13 different countries, the Handbook of Total Quality Management is invaluable as a reference guide for anyone involved with quality management and deployment, including consultants, practitioners and engineers in the professional sector, and students and lecturers of information systems, management and industrial engineering.

Introduction to Statistical Methods Design of Experiments and Statistical Quality Control

Introduction to Statistical Methods  Design of Experiments and Statistical Quality Control
Author: Dharmaraja Selvamuthu,Dipayan Das
Publsiher: Springer
Total Pages: 430
Release: 2018-09-03
ISBN 10: 9811317364
ISBN 13: 9789811317361
Language: EN, FR, DE, ES & NL

Introduction to Statistical Methods Design of Experiments and Statistical Quality Control Book Review:

This book provides an accessible presentation of concepts from probability theory, statistical methods, the design of experiments and statistical quality control. It is shaped by the experience of the two teachers teaching statistical methods and concepts to engineering students, over a decade. Practical examples and end-of-chapter exercises are the highlights of the text as they are purposely selected from different fields. Statistical principles discussed in the book have great relevance in several disciplines like economics, commerce, engineering, medicine, health-care, agriculture, biochemistry, and textiles to mention a few. A large number of students with varied disciplinary backgrounds need a course in basics of statistics, the design of experiments and statistical quality control at an introductory level to pursue their discipline of interest. No previous knowledge of probability or statistics is assumed, but an understanding of calculus is a prerequisite. The whole book serves as a master level introductory course in all the three topics, as required in textile engineering or industrial engineering. Organised into 10 chapters, the book discusses three different courses namely statistics, the design of experiments and quality control. Chapter 1 is the introductory chapter which describes the importance of statistical methods, the design of experiments and statistical quality control. Chapters 2–6 deal with statistical methods including basic concepts of probability theory, descriptive statistics, statistical inference, statistical test of hypothesis and analysis of correlation and regression. Chapters 7–9 deal with the design of experiments including factorial designs and response surface methodology, and Chap. 10 deals with statistical quality control.

Specification of Drug Substances and Products

Specification of Drug Substances and Products
Author: Christopher M. Riley,Thomas W. Rosanske,George L. Reid
Publsiher: Elsevier
Total Pages: 694
Release: 2020-07-23
ISBN 10: 0081028253
ISBN 13: 9780081028254
Language: EN, FR, DE, ES & NL

Specification of Drug Substances and Products Book Review:

Specification of Drug Substances and Products: Development and Validation of Analytical Methods, Second Edition, presents a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on phase-appropriate development, validation of analytical methods, and their application in practice. This thoroughly revised second edition covers topics not covered or not substantially covered in the first edition, including method development and validation in the clinical phase, method transfer, process analytical technology, analytical life cycle management, special challenges with generic drugs, genotoxic impurities, topical products, nasal sprays and inhalation products, and biotechnology products. The book's authors have been carefully selected as former members of the ICH Expert Working Groups charged with developing the ICH guidelines, and/or subject-matter experts in the industry, academia and in government laboratories. Presents a critical assessment of the application of ICH guidelines on method validation and specification setting Written by subject-matter experts involved in the development and application of the guidelines Provides a comprehensive treatment of the analytical methodologies used in the analysis, control and specification of new drug substances and products Covers the latest statistical approaches (including analytical quality by design) in the development of specifications, method validation and shelf-life prediction

Design for Maintainability

Design for Maintainability
Author: M. Y. L. Chew,Ashan Senel Asmone,Sheila Conejos
Publsiher: World Scientific Publishing Company
Total Pages: 164
Release: 2018-03-20
ISBN 10: 9789813232952
ISBN 13: 9813232951
Language: EN, FR, DE, ES & NL

Design for Maintainability Book Review:

With the motto of "doing it right the first time," this book focuses on spearheading the integration of designers, constructors and Facility Management, by providing easy-to-read tables summarising knowledge learned from past mistakes and maintainability benchmarks. Based on the predictive/preventive approach, the tables serve to define acceptable standards in design, construction and operation practices, to ensure the standard and quality of design, construction and maintenance practices for high maintainability at the outset of the planning/design stage. The text covers technical issues related to major components of a facility for basements, wet areas, façades, common areas, roofs and M&E.

Quality Systems Handbook

Quality Systems Handbook
Author: David Hoyle
Publsiher: Elsevier
Total Pages: 392
Release: 2015-08-11
ISBN 10: 1483104931
ISBN 13: 9781483104935
Language: EN, FR, DE, ES & NL

Quality Systems Handbook Book Review:

Quality Systems Handbook is a reference book that covers concepts and ideas in quality system. The book is comprised of two parts. Part 1 provides the background information of ISO 9000, such as its origin, composition, application, and the strategies for registration. Part 2 covers topics relevant to the ISO 9000 requirements, which include design control, internal quality audits, and statistical techniques. The text will be useful to managers, auditors, and quality practitioners who require reference in the various aspects of quality systems.

Security and Quality in Cyber Physical Systems Engineering

Security and Quality in Cyber Physical Systems Engineering
Author: Stefan Biffl,Matthias Eckhart,Arndt Lüder,Edgar Weippl
Publsiher: Springer Nature
Total Pages: 507
Release: 2019-11-09
ISBN 10: 3030253120
ISBN 13: 9783030253127
Language: EN, FR, DE, ES & NL

Security and Quality in Cyber Physical Systems Engineering Book Review:

This book examines the requirements, risks, and solutions to improve the security and quality of complex cyber-physical systems (C-CPS), such as production systems, power plants, and airplanes, in order to ascertain whether it is possible to protect engineering organizations against cyber threats and to ensure engineering project quality. The book consists of three parts that logically build upon each other. Part I "Product Engineering of Complex Cyber-Physical Systems" discusses the structure and behavior of engineering organizations producing complex cyber-physical systems, providing insights into processes and engineering activities, and highlighting the requirements and border conditions for secure and high-quality engineering. Part II "Engineering Quality Improvement" addresses quality improvements with a focus on engineering data generation, exchange, aggregation, and use within an engineering organization, and the need for proper data modeling and engineering-result validation. Lastly, Part III "Engineering Security Improvement" considers security aspects concerning C-CPS engineering, including engineering organizations’ security assessments and engineering data management, security concepts and technologies that may be leveraged to mitigate the manipulation of engineering data, as well as design and run-time aspects of secure complex cyber-physical systems. The book is intended for several target groups: it enables computer scientists to identify research issues related to the development of new methods, architectures, and technologies for improving quality and security in multi-disciplinary engineering, pushing forward the current state of the art. It also allows researchers involved in the engineering of C-CPS to gain a better understanding of the challenges and requirements of multi-disciplinary engineering that will guide them in their future research and development activities. Lastly, it offers practicing engineers and managers with engineering backgrounds insights into the benefits and limitations of applicable methods, architectures, and technologies for selected use cases.

Chemical Engineering in the Pharmaceutical Industry

Chemical Engineering in the Pharmaceutical Industry
Author: Mary T. am Ende,David J. am Ende
Publsiher: John Wiley & Sons
Total Pages: 688
Release: 2019-04-08
ISBN 10: 111928550X
ISBN 13: 9781119285502
Language: EN, FR, DE, ES & NL

Chemical Engineering in the Pharmaceutical Industry Book Review:

A guide to the important chemical engineering concepts for the development of new drugs, revised second edition The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry offers a guide to the experimental and computational methods related to drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design and process development of drug products. The authors review basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, that are addressed with consideration of the applied statistics, process analytical technology, and process control. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API’s) and 2) Drug Product Design, Development and Modeling. The contributors explore technology transfer and scale-up of batch processes that are exemplified experimentally and computationally. Written for engineers working in the field, the book examines in-silico process modeling tools that streamline experimental screening approaches. In addition, the authors discuss the emerging field of continuous drug product manufacturing. This revised second edition: Contains 21 new or revised chapters, including chapters on quality by design, computational approaches for drug product modeling, process design with PAT and process control, engineering challenges and solutions Covers chemistry and engineering activities related to dosage form design, and process development, and scale-up Offers analytical methods and applied statistics that highlight drug product quality attributes as design features Presents updated and new example calculations and associated solutions Includes contributions from leading experts in the field Written for pharmaceutical engineers, chemical engineers, undergraduate and graduation students, and professionals in the field of pharmaceutical sciences and manufacturing, Chemical Engineering in the Pharmaceutical Industry, Second Edition contains information designed to be of use from the engineer's perspective and spans information from solid to semi-solid to lyophilized drug products.

The Understanding by Design Guide to Creating High Quality Units

The Understanding by Design Guide to Creating High Quality Units
Author: Grant P. Wiggins,Jay McTighe
Publsiher: ASCD
Total Pages: 122
Release: 2011-01-01
ISBN 10: 1416611495
ISBN 13: 9781416611493
Language: EN, FR, DE, ES & NL

The Understanding by Design Guide to Creating High Quality Units Book Review:

"The Understanding by Design Guide to Creating High-Quality Units is targeted to individuals and groups interested in improving their skills in designing units of study based on the Understanding by Design (UbD) framework. This guide introduces UbD unit design and directs readers through the process. It is organized around a set of modules that move from basic ideas (e.g., the three stages of "backward design") to more complicated elements of unit design (e.g., authentic performance tasks)."--publisher website.

Indoor Air Quality Handbook

Indoor Air Quality Handbook
Author: John D. Spengler,John F. McCarthy,Jonathan M. Samet
Publsiher: McGraw Hill Professional
Total Pages: 1488
Release: 2001-01-09
ISBN 10: 0071414843
ISBN 13: 9780071414845
Language: EN, FR, DE, ES & NL

Indoor Air Quality Handbook Book Review:

* Tackles the complex environmental issue of Indoor Air Quality (IAQ) for industrial hygienists, HVAC engineers, architects and anyone else concerned with the air quality of interiors * Infused with charts, tables, and all the major formulas and calculations necessary to monitor and characterize a particular environment * Includes all relevant codes, standards and guidelines