Author: Ispe
Publisher:
ISBN: 9781931879606
Category :
Languages : en
Pages :
Book Description
ISPE Good Practice Guide: Commissioning and Qualification of Pharmaceutical Water and Steam Systems
Author: Ispe
Publisher:
ISBN: 9781931879606
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN: 9781931879606
Category :
Languages : en
Pages :
Book Description
ISPE Good Practice Guide
Author: Ispe
Publisher:
ISBN: 9781936379729
Category :
Languages : en
Pages : 116
Book Description
Publisher:
ISBN: 9781936379729
Category :
Languages : en
Pages : 116
Book Description
ISPE Good Practice Guide
Author: Ispe
Publisher:
ISBN: 9781946964175
Category :
Languages : en
Pages : 204
Book Description
Publisher:
ISBN: 9781946964175
Category :
Languages : en
Pages : 204
Book Description
ISPE Good Practice Guide
Author: Ispe
Publisher:
ISBN: 9781931879361
Category :
Languages : en
Pages : 80
Book Description
Publisher:
ISBN: 9781931879361
Category :
Languages : en
Pages : 80
Book Description
ISPE Good Practice Guide
Author: Ispe
Publisher:
ISBN: 9781936379989
Category :
Languages : en
Pages : 128
Book Description
Publisher:
ISBN: 9781936379989
Category :
Languages : en
Pages : 128
Book Description
ISPE Good Practice Guide
Author: Ispe
Publisher:
ISBN: 9781946964144
Category :
Languages : en
Pages : 148
Book Description
Publisher:
ISBN: 9781946964144
Category :
Languages : en
Pages : 148
Book Description
ISPE Guide
Author: International Society for Pharmaceutical Engineering
Publisher:
ISBN: 9781936379088
Category : Pharmaceutical industry
Languages : en
Pages : 116
Book Description
Publisher:
ISBN: 9781936379088
Category : Pharmaceutical industry
Languages : en
Pages : 116
Book Description
Analytical Method Validation and Instrument Performance Verification
Author: Chung Chow Chan
Publisher: John Wiley & Sons
ISBN: 047146371X
Category : Science
Languages : en
Pages : 320
Book Description
Validation describes the procedures used to analyze pharmaceutical products so that the data generated will comply with the requirements of regulatory bodies of the US, Canada, Europe and Japan. Calibration of Instruments describes the process of fixing, checking or correcting the graduations of instruments so that they comply with those regulatory bodies. This book provides a thorough explanation of both the fundamental and practical aspects of biopharmaceutical and bioanalytical methods validation. It teaches the proper procedures for using the tools and analysis methods in a regulated lab setting. Readers will learn the appropriate procedures for calibration of laboratory instrumentation and validation of analytical methods of analysis. These procedures must be executed properly in all regulated laboratories, including pharmaceutical and biopharmaceutical laboratories, clinical testing laboratories (hospitals, medical offices) and in food and cosmetic testing laboratories.
Publisher: John Wiley & Sons
ISBN: 047146371X
Category : Science
Languages : en
Pages : 320
Book Description
Validation describes the procedures used to analyze pharmaceutical products so that the data generated will comply with the requirements of regulatory bodies of the US, Canada, Europe and Japan. Calibration of Instruments describes the process of fixing, checking or correcting the graduations of instruments so that they comply with those regulatory bodies. This book provides a thorough explanation of both the fundamental and practical aspects of biopharmaceutical and bioanalytical methods validation. It teaches the proper procedures for using the tools and analysis methods in a regulated lab setting. Readers will learn the appropriate procedures for calibration of laboratory instrumentation and validation of analytical methods of analysis. These procedures must be executed properly in all regulated laboratories, including pharmaceutical and biopharmaceutical laboratories, clinical testing laboratories (hospitals, medical offices) and in food and cosmetic testing laboratories.
Pharmaceutical Manufacturing Handbook
Author: Shayne Cox Gad
Publisher: John Wiley & Sons
ISBN: 0470259809
Category : Science
Languages : en
Pages : 1386
Book Description
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Publisher: John Wiley & Sons
ISBN: 0470259809
Category : Science
Languages : en
Pages : 1386
Book Description
This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Microbial Limit and Bioburden Tests
Author: Lucia Clontz
Publisher: CRC Press
ISBN: 1420053493
Category : Science
Languages : en
Pages : 344
Book Description
In recent years, the field of pharmaceutical microbiology has experienced numerous technological advances, accompanied by the publication of new and harmonized compendial methods. It is therefore imperative for those who are responsible for monitoring the microbial quality of pharmaceutical/biopharmaceutical products to keep abreast of the latest c
Publisher: CRC Press
ISBN: 1420053493
Category : Science
Languages : en
Pages : 344
Book Description
In recent years, the field of pharmaceutical microbiology has experienced numerous technological advances, accompanied by the publication of new and harmonized compendial methods. It is therefore imperative for those who are responsible for monitoring the microbial quality of pharmaceutical/biopharmaceutical products to keep abreast of the latest c