This book focuses on sterilizing grade filters in the biopharmaceutical industry, emphasizing practical applications of universal and dependable operational protocols, integrity testing, and troubleshooting to streamline the production and preparation of pharmaceuticals.
Addresses the complexities of globalizing redundancy in filtration!
Enabling educated developmental, procedural, and regulatory judgments to be made in the manufacturing of sterile health care products, Sterile Filtration
considers how many filters should be in the process streamexamines the existence of nanobacteria and viable but nonculturable organismscovers pore size designations, distributions, architecture, and numbersdiscusses the latest findings in bubble point and diffuse flow measurementsdescribes pre- and postfiltration, up- and downstream testing, and after-stream sterilizationsdetails wetting liquid, polymer, temperature, and water purity effectsexplains sieve retention, size exclusion, adsorptive sequestrations, charge-related phenomena, gravitational settling, and interference factors in liquids and gasesoutlines filter validation, requirements, and operational specificsand more!
Advocating separation in addition to physical destruction of microorganisms, Sterile Filtration is a reference essential for pharmaceutical scientists; biotechnologists; microbiologists; virologists; process and chemical engineers; plant, production, validation, and quality control managers in the pharmaceutical and biotechnology industries; and upper-level undergraduate and graduate school students in these disciplines.
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