IEST RP-CC023 2-2006 MICROORGANISMS IN CLEANROOMS.pdf
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1、INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Contamination Control Division Reco ended Practice C023.2 IEST-RP-C023.2 Microrganisms in Cleanroms INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Arlington Place One 2340 S. Arlington Heights Road, Suite 10 Arlington Heights, IL 6005-4516 Phone
2、: (847) 981-010 Fax: (847) 981-4130 E-mail: iestiest.org Web: ww.iest.org 2 Copyrighted material INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY IEST-RP-C023.2 IEST-RP-C023.2 INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Copyrighted material 3 This Recomended Practice is published by the INS
3、TITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY to advance the technical and enginering sciences. Its use is entirely voluntary, and determination of its aplicability and suitability for any particular use is solely the responsibility of the user. This Recomended Practice was prepared by and is unde
4、r the jurisdiction of Working Group 023 of the IEST Con-tamination Control Division. Copyright 206 by the INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY First printing, January 206 ISBN 978-0-9747313-6-0 PROPOSAL FOR IMPROVEMENT: The Working Groups of the INSTITUTE OF ENVIRONMENTAL SCIENCES AND
5、TECHNOLOGY are continualy working on improvements to their Recomended Practices and Reference Documents. Sugestions from those who use these documents are welcome. If you have a sugestion regarding this document, please use the online Proposal for Improvement form found on the IEST website at ww.ies
6、t.org/proposal/form.html. INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Arlington Place One 2340 S. Arlington Heights Road, Suite 10 Arlington Heights, IL 6005-4516 Phone: (847) 981-010 Fax: (847) 981-4130 E-mail: iestiest.org Web: ww.iest.org 4 Copyrighted material INSTITUTE OF ENVIRONMENTAL S
7、CIENCES AND TECHNOLOGY IEST-RP-C023.2 IEST-RP-C023.2 INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Copyrighted material 5 Microorganisms in Cleanrooms IEST-RP-C023.2 CONTENTS SECTION 1 SCOPE AND LIMITATIONS.7 2 REFERENCES7 3 TERMS AND EFINITIONS.8 4 BACKGROUND AND PURPOSE10 5 MICROBIAL CONTROL
8、STRATEGY1 6 ENVIRONMENTAL CONTAMINATION CONTROL.13 7 DESIGN/IMPLEMENTATION OF PERSONEL CONTAMINATION CONTROL PROCEDURES14 8 ESTABLISHING AN EFECTIVE CLEANROM CLEANING PROGRAM17 9 DESIGN/IMPLEMENTATION OF AN ENVIRONMENTAL MONITORING PROGRAM.21 FIGURE 1 PROCES FOR DETERMINING REQUIRED CONTROL STRATEGI
9、ES.12 TABLE 1 GOWNING CONFIGURATIONS.14 2 TYPICAL ASEPTIC GOWNING PROCEDURE15 3 DISINFECTANT GUIDE18 4 CHARACTERISTICS OF VARIOUS TYPES OF MICROBIOLOGICAL AIR SAMPLING EQUIPMENT.26 5 APROPRIATE RECOVERY MEDIA, INCUBATION CONDITIONS, AND INCUBATION TIMES FOR COMON ENVIRONENTAL ORGANISM TYPES29 APPEND
10、IX A BIBLIOGRAPHY30 6 Copyrighted material INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY IEST-RP-C023.2 IEST-RP-C023.2 INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Copyrighted material 7 INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY Contamination Control Division Recommended Practice
11、 023.2 Microorganisms in Cleanrooms IEST-RP-C023.2 1 SCOPE AND LIMITATIONS 1.1 Scope This Recomended Practice (RP) provides guidelines for the control and quantitative measurement of viable contamination in the air and on surfaces in environ-ments that require control of such contamination. This inc
12、ludes areas designated as aseptic and those consid-ered nonsterile. The procedures and techniques em-ployed to achieve the desired level of microbial control are dependent on the level of bioburden that can be tolerated. This RP presents an introduction to the cur-rently acepted methods for bioburde
13、n control and environmental monitoring as wel as the devices avail-able for the quantification of airborne and surface vi-able contamination. This document also describes disinfectants, their le-thality spectrum, and techniques for their aplication. 1.2 Limitations Any controled area designated for
14、the manufacture or storage of a medical device, pharmaceutical product, or fod product is subject to regulations imposed by agencies that govern each industry. This document is not intended to supersede or substitute for these regula-tions. It is intended to provide a framework for met-ing the regul
15、atory requirements and to achieve the highest level of bioburden control required for other types of environments. In selecting a disinfectant, it is the responsibility of the user to consider al factors related to but not necesar-ily limited to personel safety, aplication devices, methods, surface
16、compatibility, residues, and bacteri-cidal or bacteriostatic eficiency. The selection of testing and disinfection methods var-ies with the desired level of airborne and surface bioburden. 2 REFERENCES The cited editions of the folowing documents are in-corporated into this RP to the extent specified
17、 herein. Users are encouraged to investigate the posibility of aplying the most recent editions of the references. 2.1 Documents ANSI/AMI/ISO 1137194 Sterilization of health care productsRequirements for validation and rou-tine controlRadiation sterilization ANSI/AMI/ISO 1737-1195 Sterilization of m
18、edi-cal devicesMicrobiological methodsPart 1: Esti-mation of population of microrganisms on products Asociation of Oficial Analytical Chemists. The Ofi-cial Methods of Analysis of AOAC International 18th Ed., Chapter 6, p. 4, 7, 8. Guidance for Industry Sterile Drug Products Produced by Aseptic Proc
19、esingCurent God Manufacturing Practice. September 204. US Fod and Drug Ad-ministration. IEST-RP-C03: Garment System Considerations For Cleanroms and Other Controled Environments IEST-RP-C018: Cleanrom Housekeping: Operat-ing and Monitoring Procedures IEST-RP-C034: HEPA and ULPA Filter Leak Tests ISO
20、 1464-1 Cleanroms and asociated controled environmentsPart 1: Clasification of air cleanlines ISO 1464-4 Cleanroms and asociated controled environmentsPart 4: Design, construction and start-up ISO 14698-1 Cleanroms and asociated controled environmentsBiocontamination controlPart 1: General principle
21、s and methods ISO/DTR 14698-3 Cleanroms and asociated con-troled environmentsBiocontamination controlPart 3: Measurement of the eficiency of proceses of 8 Copyrighted material INSTITUTE OF ENVIRONMENTAL SCIENCES AND TECHNOLOGY IEST-RP-C023.2 cleaning and/or disinfection of inert surfaces bearing bio
22、contaminated wet soiling or biofilms Parenteral Drug Asociation Task Force on Decon-taminating Agents. 1986. Decontaminated Agents. Journal of Parenteral Science and Technology 40 (3): 104-109 Parenteral Drug Asociation. Technical Report #13Fundamentals of an Environmental Monitoring Program US Air
23、Force. December 1, 1972. Technical Order 0-25-203 Contamination Control of Aerospace Facilities, (ww.robins.af.mil/logistics/LGEDA/Documents/ 0series.htm) USP 29NF 24 United States PharmacopeiaNational Formulary January 1, 206 2.2 Sources and Addresses ANSI American National Standards Institute 25 W
24、est 43rd Stret New York, NY 1036, USA Phone: 212-642-490 Fax: 212-398-023 ww.ansi.org AMI Asociation for the Advancement of Medical Instrumentation 110 North Glebe Road, Suite 20 Arlington, VA 2201-4795 Phone: 703-525-4890 Fax: 703-276-0793 ww.ami.org AOAC Asociation of Oficial Analytical Chemists 4
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