ISPE Good Practice Guide: Commissioning and Qualification of Pharmaceutical Water and Steam Systems

ISPE Good Practice Guide: Commissioning and Qualification of Pharmaceutical Water and Steam Systems PDF Author: Ispe
Publisher:
ISBN: 9781931879606
Category :
Languages : en
Pages :

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ISPE Good Practice Guide: Commissioning and Qualification of Pharmaceutical Water and Steam Systems

ISPE Good Practice Guide: Commissioning and Qualification of Pharmaceutical Water and Steam Systems PDF Author: Ispe
Publisher:
ISBN: 9781931879606
Category :
Languages : en
Pages :

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Book Description


ISPE Good Practice Guide

ISPE Good Practice Guide PDF Author: Ispe
Publisher:
ISBN: 9781936379729
Category :
Languages : en
Pages : 116

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Book Description


ISPE Good Practice Guide

ISPE Good Practice Guide PDF Author: Ispe
Publisher:
ISBN: 9781946964175
Category :
Languages : en
Pages : 204

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ISPE Good Practice Guide

ISPE Good Practice Guide PDF Author: Ispe
Publisher:
ISBN: 9781931879361
Category :
Languages : en
Pages : 80

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Book Description


ISPE Good Practice Guide

ISPE Good Practice Guide PDF Author: Ispe
Publisher:
ISBN: 9781936379989
Category :
Languages : en
Pages : 128

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ISPE Good Practice Guide

ISPE Good Practice Guide PDF Author: Ispe
Publisher:
ISBN: 9781946964144
Category :
Languages : en
Pages : 148

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ISPE Guide

ISPE Guide PDF Author: International Society for Pharmaceutical Engineering
Publisher:
ISBN: 9781936379088
Category : Pharmaceutical industry
Languages : en
Pages : 116

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Book Description


Analytical Method Validation and Instrument Performance Verification

Analytical Method Validation and Instrument Performance Verification PDF Author: Chung Chow Chan
Publisher: John Wiley & Sons
ISBN: 047146371X
Category : Science
Languages : en
Pages : 320

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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

Pharmaceutical Manufacturing Handbook PDF Author: Shayne Cox Gad
Publisher: John Wiley & Sons
ISBN: 0470259809
Category : Science
Languages : en
Pages : 1386

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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

Microbial Limit and Bioburden Tests PDF Author: Lucia Clontz
Publisher: CRC Press
ISBN: 1420053493
Category : Science
Languages : en
Pages : 344

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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