Kimmuh.com

Informa Healthcare | August 31, 1990 | ISBN-10: 0824783441 | 368 pages | PDF | 4 MB Reviews the properties, synthesis, and formulations of a number of well studied polymers increasingly being used in site-specific or systematic administration of pharmaceutical agents. For each of the polymers, discusses the background; chemistry and synthesis.

Table of Contents: Articles Increased Process Understanding Through Monitoring and Scale-Down Models: Case Study of a Cell Culture Harvest Fluid Titration and Filtration Process by Kurt Yanagimachi, Corey Dodge, and Marisa Hewitt This article presents a case study demonstrating the use of detailed process monitoring and scale-down modeling in determining the root causes of yield […]

The Handbook of Membrane Separations: Chemical, Pharmaceutical, and Biotechnological Applications provides detailed information on membrane separation technologies as they have evolved over the past decades. To provide a basic understanding of membrane technology, this book documents the developments dealing with these technologies. It explores chemical, pharmaceutical, food processing and biotechnological applications of membrane processes ranging […]

Completely revised and updated to reflect the significant advances in pharmaceutical production and regulatory expectations, this third edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and competitive. The many chapters added to the prior compilation examine validation and six sigma system design; the preparation […]

Thoroughly updated and expanded, this new 3rd edition provides the latest information on dosage, forms, film defects, and polymer characterization. Written by renowned leaders in the field, Aqueous Polymeric Coatings for Pharmaceutical Dosage Formsis easily the most comprehensive book available on the market today.New to the 3rd Edition:

The Pharmaceutical Engineering Series is a comprehensive reference for the pharmaceutical professional covering all aspects from quality, documentation and validation through manufacturing processes to facility design and management. In ‘Quality’, Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the quality life cycle, management and cost of quality, GMP, auditing […]

Pharmaceutical Engineering – May/June 2008 Table of Contents Articles A Risk-Based Approach to Cleaning Validation using Visible Residue Limits by Richard J. Forsyth and Jeffrey L. Hartman This article describes the development of a Visible Residue Limits (VRL) program in a pharmaceutical manufacturing facility, including sample and viewing parameters. Opportunities for VRL implementation were identified […]