Author: Jack O'Grady
Publisher:
ISBN:
Category : Biology
Languages : en
Pages :
Book Description
Quality Assurance & Regulatory Affairs for the Biosciences
Author: Jack O'Grady
Publisher:
ISBN:
Category : Biology
Languages : en
Pages :
Book Description
Publisher:
ISBN:
Category : Biology
Languages : en
Pages :
Book Description
Quality Assurance and Regulatory Affairs for the Biosciences
Author: Jack O'Grady
Publisher:
ISBN:
Category :
Languages : en
Pages : 207
Book Description
A solid and attractive book to learn. More than a compilation book of standards and techniques, this book provides a real and clear guide to learning about quality assurance and regulatory issues of pharmaceutical, biomedical and biotechnological products. In this short book, Jack O'Grady introduces dynamically and consistently the topics of greatest interest to the reader. Also, a series of links to the web pages of the relevant institutions (eg manuals, guides, statistics) is provided through scannable QR codes, thus granting a greater utility to the reader and reducing redundant and technical content to make reading more agile and productive. Table of Contents: Chapter 1. Introduction to Biotechnology and Quality Assurance. Chapter 2. Introduction to Quality Principles Chapter 3. Quality Management Systems Chapter 4. The Food and Drug Administration Chapter 5. Good Guidance Practices (GXPs) Chapter 6. The Drug Approval Process Chapter 7. The Regulation of Biologics Chapter 8. Medical Device and Combination Products Chapter 9. Regulation of Food and Other Products Chapter 10. FDA Enforcement ⚠ Before purchasing this book, consider: This book is not designed for experts in the field, as it may fall into the basics. This book is not a compendium of regulations but provides links to find them on the websites of the relevant institutions. This book does not compile analytical laboratory techniques. Instead, it explains the management of quality standards and management of product quality at the corporate level. This book is short and does not provide an exhaustive discussion of all the topics, however, it does provide a solid basis for the reader to delve into his interests.
Publisher:
ISBN:
Category :
Languages : en
Pages : 207
Book Description
A solid and attractive book to learn. More than a compilation book of standards and techniques, this book provides a real and clear guide to learning about quality assurance and regulatory issues of pharmaceutical, biomedical and biotechnological products. In this short book, Jack O'Grady introduces dynamically and consistently the topics of greatest interest to the reader. Also, a series of links to the web pages of the relevant institutions (eg manuals, guides, statistics) is provided through scannable QR codes, thus granting a greater utility to the reader and reducing redundant and technical content to make reading more agile and productive. Table of Contents: Chapter 1. Introduction to Biotechnology and Quality Assurance. Chapter 2. Introduction to Quality Principles Chapter 3. Quality Management Systems Chapter 4. The Food and Drug Administration Chapter 5. Good Guidance Practices (GXPs) Chapter 6. The Drug Approval Process Chapter 7. The Regulation of Biologics Chapter 8. Medical Device and Combination Products Chapter 9. Regulation of Food and Other Products Chapter 10. FDA Enforcement ⚠ Before purchasing this book, consider: This book is not designed for experts in the field, as it may fall into the basics. This book is not a compendium of regulations but provides links to find them on the websites of the relevant institutions. This book does not compile analytical laboratory techniques. Instead, it explains the management of quality standards and management of product quality at the corporate level. This book is short and does not provide an exhaustive discussion of all the topics, however, it does provide a solid basis for the reader to delve into his interests.
Fundamentals of Biomaterials
Author: Vasif Hasirci
Publisher: Springer Nature
ISBN: 3031540468
Category :
Languages : en
Pages : 406
Book Description
Publisher: Springer Nature
ISBN: 3031540468
Category :
Languages : en
Pages : 406
Book Description
Quality Assurance for Biopharmaceuticals
Author: Jean F. Huxsoll
Publisher: Wiley-Interscience
ISBN:
Category : Medical
Languages : en
Pages : 222
Book Description
Dr. Jean Huxsoll and a team of distinguished biotechnology industry experts from the U.S. and Europe offer a wealth of practical guidelines to designing, implementing, and managing QA systems to assure that biopharmaceutical products meet standards for safety purity, and potency. Quality Assurance for Biopharmaceuticals covers all important theoretical and practical concerns, including detailed guidelines to meeting GMP compliance; quality assurance of production; quality assurance of analytical methods; advanced documentation, sampling, and validation techniques; comprehensive coverage of regulatory issues in the U.S., Europe, and Japan; and much more.
Publisher: Wiley-Interscience
ISBN:
Category : Medical
Languages : en
Pages : 222
Book Description
Dr. Jean Huxsoll and a team of distinguished biotechnology industry experts from the U.S. and Europe offer a wealth of practical guidelines to designing, implementing, and managing QA systems to assure that biopharmaceutical products meet standards for safety purity, and potency. Quality Assurance for Biopharmaceuticals covers all important theoretical and practical concerns, including detailed guidelines to meeting GMP compliance; quality assurance of production; quality assurance of analytical methods; advanced documentation, sampling, and validation techniques; comprehensive coverage of regulatory issues in the U.S., Europe, and Japan; and much more.
Quality Assurance and Regulatory Affairs for the Biosciences
Author: Jack O'Grady
Publisher:
ISBN:
Category :
Languages : en
Pages : 207
Book Description
A solid and attractive book to learn. More than a compilation book of standards and techniques, this book provides a real and clear guide to learning about quality assurance and regulatory issues of pharmaceutical, biomedical and biotechnological products. In this short book, Jack O'Grady introduces dynamically and consistently the topics of greatest interest to the reader. Also, a series of links to the web pages of the relevant institutions (eg manuals, guides, statistics) is provided through scannable QR codes, thus granting a greater utility to the reader and reducing redundant and technical content to make reading more agile and productive. Table of Contents: Chapter 1. Introduction to Biotechnology and Quality Assurance. Chapter 2. Introduction to Quality Principles Chapter 3. Quality Management Systems Chapter 4. The Food and Drug Administration Chapter 5. Good Guidance Practices (GXPs) Chapter 6. The Drug Approval Process Chapter 7. The Regulation of Biologics Chapter 8. Medical Device and Combination Products Chapter 9. Regulation of Food and Other Products Chapter 10. FDA Enforcement ⚠ Before purchasing this book, consider: This book is not designed for experts in the field, as it may fall into the basics. This book is not a compendium of regulations but provides links to find them on the websites of the relevant institutions. This book does not compile analytical laboratory techniques. Instead, it explains the management of quality standards and management of product quality at the corporate level. This book is short and does not provide an exhaustive discussion of all the topics, however, it does provide a solid basis for the reader to delve into his interests.
Publisher:
ISBN:
Category :
Languages : en
Pages : 207
Book Description
A solid and attractive book to learn. More than a compilation book of standards and techniques, this book provides a real and clear guide to learning about quality assurance and regulatory issues of pharmaceutical, biomedical and biotechnological products. In this short book, Jack O'Grady introduces dynamically and consistently the topics of greatest interest to the reader. Also, a series of links to the web pages of the relevant institutions (eg manuals, guides, statistics) is provided through scannable QR codes, thus granting a greater utility to the reader and reducing redundant and technical content to make reading more agile and productive. Table of Contents: Chapter 1. Introduction to Biotechnology and Quality Assurance. Chapter 2. Introduction to Quality Principles Chapter 3. Quality Management Systems Chapter 4. The Food and Drug Administration Chapter 5. Good Guidance Practices (GXPs) Chapter 6. The Drug Approval Process Chapter 7. The Regulation of Biologics Chapter 8. Medical Device and Combination Products Chapter 9. Regulation of Food and Other Products Chapter 10. FDA Enforcement ⚠ Before purchasing this book, consider: This book is not designed for experts in the field, as it may fall into the basics. This book is not a compendium of regulations but provides links to find them on the websites of the relevant institutions. This book does not compile analytical laboratory techniques. Instead, it explains the management of quality standards and management of product quality at the corporate level. This book is short and does not provide an exhaustive discussion of all the topics, however, it does provide a solid basis for the reader to delve into his interests.
Research on the Management of Innovation
Author: Andrew H. Van de Ven
Publisher: Oxford University Press
ISBN: 0195349911
Category : Business & Economics
Languages : en
Pages : 751
Book Description
This is a reprint of a classic work of research on innovation first published in 1989. Resulting from the Minnesota Innovation Research Program (MIRP), the book includes a revised and expanded Preface and will complement the three other books growing out of the program, all published by Oxford--The Innovation Journey (1999), Organizational Change Processes: Theory and Methods for Research (2000), and Handbook of Organizational Change and Development (coming 2001).
Publisher: Oxford University Press
ISBN: 0195349911
Category : Business & Economics
Languages : en
Pages : 751
Book Description
This is a reprint of a classic work of research on innovation first published in 1989. Resulting from the Minnesota Innovation Research Program (MIRP), the book includes a revised and expanded Preface and will complement the three other books growing out of the program, all published by Oxford--The Innovation Journey (1999), Organizational Change Processes: Theory and Methods for Research (2000), and Handbook of Organizational Change and Development (coming 2001).
Expertise in Regulation and Law
Author: Gary Edmond
Publisher: Routledge
ISBN: 1351937723
Category : Law
Languages : en
Pages : 340
Book Description
This collection of essays examines the multi-faceted roles of experts and expertise in and around contemporary legal and regulatory cultures. The essays illustrate the complexity intrinsic to the production and use of expert knowledge, particularly during transition from specialist communities to other domains such as policy formulation, regulatory standard setting and litigation. Several themes pervade the collection. These include the need to recognize that: expert knowledge and opinion is often complex, controversial and contested; there are no simple criteria for resolving disagreements between experts; appeals to 'objectivity' and 'impartiality' tend to be rhetorical rather than analytical; contests in expertise are frequently episodes in larger campaigns; there are many different models of expertise and knowledge; processes designed to deal with expert knowledge are unavoidably political; questions around who is an expert and what should count as expertise are not always self-evident; and the evidence rarely 'speaks for itself'.
Publisher: Routledge
ISBN: 1351937723
Category : Law
Languages : en
Pages : 340
Book Description
This collection of essays examines the multi-faceted roles of experts and expertise in and around contemporary legal and regulatory cultures. The essays illustrate the complexity intrinsic to the production and use of expert knowledge, particularly during transition from specialist communities to other domains such as policy formulation, regulatory standard setting and litigation. Several themes pervade the collection. These include the need to recognize that: expert knowledge and opinion is often complex, controversial and contested; there are no simple criteria for resolving disagreements between experts; appeals to 'objectivity' and 'impartiality' tend to be rhetorical rather than analytical; contests in expertise are frequently episodes in larger campaigns; there are many different models of expertise and knowledge; processes designed to deal with expert knowledge are unavoidably political; questions around who is an expert and what should count as expertise are not always self-evident; and the evidence rarely 'speaks for itself'.
7 Fundamentals of an Operationally Excellent Management System
Author: Chitram Lutchman
Publisher: CRC Press
ISBN: 1482205777
Category : Business & Economics
Languages : en
Pages : 444
Book Description
Developing and maintaining a disciplined management system provides any organization with a blueprint for exceptional performance and success. Indeed, for larger multinational corporations, a management system is a critical component for sustainable growth and performance management. In this book, the authors discuss a series of fundamentals for cr
Publisher: CRC Press
ISBN: 1482205777
Category : Business & Economics
Languages : en
Pages : 444
Book Description
Developing and maintaining a disciplined management system provides any organization with a blueprint for exceptional performance and success. Indeed, for larger multinational corporations, a management system is a critical component for sustainable growth and performance management. In this book, the authors discuss a series of fundamentals for cr
Plunkett's Biotech & Genetics Industry Almanac
Author: Jack W. Plunkett
Publisher: Plunkett Research, Ltd.
ISBN: 1593921241
Category :
Languages : en
Pages : 602
Book Description
A complete market research guide to the business of biotech, genetics, proteomics and related services--a tool for strategic planning, competitive intelligence, employment searches, or financial research. Complete profiles of nearly 400 leading biotech companies, in-depth chapters on trends. Includes glossary thorough indexes, statistics, research and development, emerging technology--as well a addresses, phone numbers, and executive names.
Publisher: Plunkett Research, Ltd.
ISBN: 1593921241
Category :
Languages : en
Pages : 602
Book Description
A complete market research guide to the business of biotech, genetics, proteomics and related services--a tool for strategic planning, competitive intelligence, employment searches, or financial research. Complete profiles of nearly 400 leading biotech companies, in-depth chapters on trends. Includes glossary thorough indexes, statistics, research and development, emerging technology--as well a addresses, phone numbers, and executive names.
Safety Management
Author: Chitram Lutchman
Publisher: CRC Press
ISBN: 1439862621
Category : Business & Economics
Languages : en
Pages : 488
Book Description
With annual cost in excess of $150 billion from workplace related illnesses and injuries, any knowledge that can reduce this burden contributes to the overall welfare of the work force and business performance. Yet, there are many key areas of opportunities that have not yet been discussed in the literature, such as approaches to improving contract
Publisher: CRC Press
ISBN: 1439862621
Category : Business & Economics
Languages : en
Pages : 488
Book Description
With annual cost in excess of $150 billion from workplace related illnesses and injuries, any knowledge that can reduce this burden contributes to the overall welfare of the work force and business performance. Yet, there are many key areas of opportunities that have not yet been discussed in the literature, such as approaches to improving contract