Microbial contamination control in the pharmaceutical industry

Cover of: Microbial contamination control in the pharmaceutical industry |

Published by Marcel Dekker in New York .

Written in English

Read online

Subjects:

  • Drugs -- Microbiology.,
  • Microbial contamination -- Prevention.,
  • Pharmaceutical industry -- Quality control.

Edition Notes

Includes index.

Book details

Statementedited by Luis Jiminez.
SeriesDrugs and the pharmaceutical sciences ;, 142
ContributionsJiménez, Luis.
Classifications
LC ClassificationsRS199.M53 M527 2004
The Physical Object
Paginationvii, 310 p. :
Number of Pages310
ID Numbers
Open LibraryOL3328576M
ISBN 10082475753X
LC Control Number2004303347
OCLC/WorldCa56539121

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Microbial Contamination Control in the Pharmaceutical Industry - CRC Press Book. This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and procedures used to prevent the microbial contamination of pharmaceutical processes, products, and environments.

With more than tables and current references, the book contains a detailed analysis of microbial contamination recalls for nonsterile and sterile pharmaceutical products, demonstrating the.

With more than tables and current references, the book contains a detailed analysis of microbial contamination recalls for nonsterile and sterile pharmaceutical products, demonstrating the distribution of microorganisms worldwide and the identification by geographical oazadlaciebie.com: Luis Jimenez.

Pharmaceutical microbiology is a specialist area of microbiology and one concerned with the use of microorganisms in pharmaceutical development and with maintaining contamination control. This chapter introduces the subject and outlines some the typical tests conducted within a pharmaceutical microbiology laboratory (such as microbial limits.

MICROBIAL CONTAMINATION CONTROL IN THE PHARMACEUTICAL INDUSTRY by JIMENEZ LUIS and a great selection of related books, art and collectibles available now at oazadlaciebie.com Note: Citations are based on reference standards.

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Jones, in Shellfish Safety and Quality, Abstract: Microbial contamination is a challenging and significant issue for the shellfish industry.

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To prevent microbial contamination, these facilities, materials, and personnel should provide an environment that will minimize the survival, growth, and distribution of microorganisms.

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D.;] -- This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and procedures used to prevent the microbial contamination of. Contamination control in pharmaceutical clean rooms has developed from a jumble of science and engineering, knowledge of what has worked well or badly in the past, dependent upon the technology available at the time the clean room was built and subsequent technological developments.

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Microorganisms may cause health-threatening conditions directly by being. So, how do we effectively apply microbial controlSo, how do we effectively apply microbial control in the manufacture of non-sterile products.

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Microbial Contamination Control in the Pharmaceutical Industry bookCited by: 8. Oct 05,  · This study has revealed heavy microbial contamination in 50% of pharmaceuticals dispensed at our hospital pharmacy.

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Contamination Control in Healthcare Manufacturing (book) The latest in the series from Masden and Moldenhauer is available, covering such key topics as Regulatory.

Microbial contamination control remains a critical focus for the pharmaceutical industry. Microbial controls can be found throughout the manufacturing process including, but not limited to, raw materials, equipment, cleanroom environments, finished product manufacturing, and.

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With both sterile and non-sterile products, the effects can range from discoloration to the potential for fatality. Oct 10,  · This review gives a brief overview about microbial contamination in pharmaceutical products. We discuss the distribution and potential sources of microorganisms in different areas, ranging from manufacturing sites, pharmacy stores, hospitals, to the post-market phase.

We also discuss the factors that affect microbial contamination in popular dosage forms (e.g., tablets, sterile products Cited by: 7.

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Microbial Aspects in Cleaning Validation. Contamination Control in the Pharmaceutical Industry procedures used to prevent the microbial contamination of pharmaceutical processes, products.

Mar 07,  · The most important contribution of microbiology to the pharmaceutical industry is the development of antibiotics. All antibiotics were originally the products of microbial metabolism, however the recent genetic manipulations have enabled the production of more enhanced drugs.

Sep 01,  · Good Practices in the Biopharmaceutical Industry. Because bio/pharmaceutical products are generally intended for ill populations, bioburden control throughout the whole manufacturing plant should be maintained effectively to minimize the risk of medicinal products contamination.

Special Indian Reprint. Microbial Contamination Control in the Pharmaceutical Industry edited by Luis Jimenez. Microbial Contamination Control in the Pharmaceutical Industry presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and procedures used to prevent the microbial contamination of pharmaceutical processes, products, and environments.

Pharmaceutical Contamination Control Ankur Choudhary Print Question Forum No comments Introduction of undesired dust or dirt into or on to during manufacturing, packing and transportation is called as contamination and contaminant is the unwanted element being introduced in the system.

Feb 27,  · 1. Contamination Control in Pharmaceutical Industry Maintaining sterility and contamination control are important factors in any of the pharmaceutical industry. Most, if not all chemicals naturally contain some degree of contamination, however, even low levels of contaminants can be expensive or possibly hazardous.

With more than tables and current references, the book contains a detailed analysis of microbial contamination recalls for nonsterile and sterile pharmaceutical products, demonstrating the distribution of microorganisms worldwide and the identification by geographical regions.

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Jun 16,  · Microbial contamination in pharmaceutical products has massive consequences. Karla Fjeld explains what we can do to optimise our QC and help. Oct 28,  · The Pharmaceutical and Healthcare Sciences Society (PHSS) has prepared a whitepaper on control strategies for sterile pharmaceutical/drug product manufacture and this article uses extracts to highlight the increasing requirements for control strategies in Author: James Drinkwater.

Preventing Cross Contamination In Pharmaceutical Production Process. Check that every material is free from microbial or any other form of contamination. Before using, remove the outer wrapping of the packaging material to help reduce contamination.

Different Types Of Contamination, Causes And Prevention For Pharmaceutical Industry. Contamination control for a non-sterile drug was first highlighted by Professor Kallings 1 in Sweden in He detected strains of Salmonella in an oral drug, Thyroidinum, USP, a dry thyroid powder from domestic animals.

At this time there were no microbial specifications for non-sterile drugs or cosmetics. Microbial contamination. Microbiological contamination refers to the non-intended or accidental introduction of microbes such as bacteria, yeast, mould, fungi.

Jun 02,  · In both cases, contamination control is more problematic and, consequently, the drugmanufacturing process is more difficult to manage. The most common approach to microbial control problems due to facility design flaws or damage is to increase the use of chemical antimicrobial products by concentration, frequency, or both.

Aug 20,  · Microbial Control. Microbiological contamination is a major concern for pharmaceutical water. The presence of microbes, including bacteria and their endotoxins, is inevitable.

Microbes are found in any and all water systems, and they are unpredictable.Conclusion: Testing conditions and challenges could be overcome for recovery and detection of microbial contaminants in collected non sterile pharmaceutical preparations. The microbiological quality of the examined products was, in general, adequate with the exception of few oazadlaciebie.com by: 4.The potential impact of such contamination can be catastrophic.

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