Quality Assurance

PUBLISHED


Viewing: 1 - 10 of 70
Published:
December 15, 2012
Editor(s):
Sandeep Nema; John D. Ludwig
This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it 
  Hardback
$259.95
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Published:
December 15, 2012
Editor(s):
Sandeep Nema; John D. Ludwig
This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it 
  Hardback
$259.95
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Published:
June 06, 2012
Author(s):
Syed Imtiaz Haider; Erfan Syed Asif
To stay in compliance with regulations, pharmaceutical, medical, and biotech companies must create qualtiy SOPs that build in the regulatory requirements into actions and describe personal flow, internal flow, flow of information, and processing steps. Quality Operations Procedures for 
  Hardback
$129.95
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Published:
November 17, 2011
Author(s):
William J. Mead
Dietary Supplement GMP is a one-stop "how-to" road map to the final dietary supplement GMP regulations recently issued by the FDA covering the manufacture, packaging, and holding of dietary supplement products. The recent regulations, outlining broad goals, intentionally avoid specifics to allow 
  Hardback
$159.95
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Published:
July 27, 2011
Editor(s):
Steven W. Baertschi; Karen M. Alsante; Robert A. Reed
The second edition of Pharmaceutical Stress Testing: Predicting Drug Degradation provides a practical and scientific guide to designing, executing and interpreting stress testing studies for drug substance and drug product. This is the only guide available to tackle this subject in-depth. The 
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$259.95
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Published:
February 16, 2011
Author(s):
Syed Imtiaz Haider; Syed Erfan Asif
Written to help companies comply with GMP, GLP, and validation requirements imposed by the FDA and regulatory bodies worldwide, Quality Control Training Manual: Comprehensive Training Guide for API, Finished Pharmaceutical and Biotechnologies Laboratories presents cost-effective training courses 
  Hardback
$146.95
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Published:
August 20, 2010
Author(s):
Michael J. Akers
Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high quality sterile dosage forms. The author has 38 years of experience in the development and manufacture of sterile dosage forms including solutions, 
  Hardback
$219.95
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Published:
July 23, 2010
Editor(s):
James Agalloco; James Akers
The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has witnessed continual improvement over the last half century. New approaches that have transformed classical aseptic production methods are appearing 
  Hardback
$339.95
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Published:
February 23, 2010
Editor(s):
Guy Wingate
Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements 
  Hardback
$471.00
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Published:
May 28, 2009
Editor(s):
Alexander T. Florence; Juergen Siepmann
With over 100 illustrations, Volume 1 addresses the core disciplines of pharmaceutics (absorption, PK, excipients, tablet dosage forms, and packaging), and explores the challenges and paradigms of pharmaceutics.Key topics in Volume 1 include:• principles of drug absorption, chemical kinetics, and 
  Hardback
$139.95
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