[Openflow-dev] Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated compan

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<DIV align=center><A class=headingtxt href="http://email.complianceonline.com/cgi-bin18/DM/t/hY3D0V3H340PrQ0rmT0Er" target=_blank><U>Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies</U> </A></DIV></TD>
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<TD class=text2 colSpan=3 height=24><EM>by Jim Polarine</EM></TD>
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<DIV align=center><SPAN class=text1><STRONG><SPAN class=title4><A class=style24 href="http://email.complianceonline.com/cgi-bin18/DM/t/hY3D0V3H340PrQ0rmU0Es" target=_blank><U>Buy Training CD</U></A></SPAN> </STRONG></SPAN><SPAN class=style25>(</SPAN><SPAN class=text1><STRONG>30% off</STRONG>. Use coupon code <STRONG>115770, </STRONG>valid till Dec 24, 2010)</SPAN></DIV></TD>
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<P class=text1>This Disinfection and Cleanroom Cleaning training will teach you how to choose the best disinfectants, know the different performance parameters of disinfectants, methods to qualify disinfectants, writing and executing cleaning procedures. </P>
<P class=style20 align=left><STRONG><STRONG>Areas Covered in the Seminar:</STRONG></STRONG></P>
<UL>
<LI class=text>Disinfectants commonly used in the industry, their modes of action, efficacy, and toxicity. 
<LI class=text>Understanding the nature of contaminants in the cleanroom and which disinfectants will be effective against them. 
<LI class=text>Benefits and drawbacks for using each type of disinfectant used in the Pharmaceutical Industry. 
<LI class=text>Bodies that regulate disinfectant manufacturers and testing required by manufacturer's for label claim. 
<LI class=text>Learn disinfectant testing methodologies. 
<LI class=text>Review of &#8220real world&#8221 examples of disinfectant efficacy tests. 
<LI class=text>Troubleshooting problems related to disinfectant efficacy testing. 
<LI class=text>Overview of the many methods and variations used for disinfectant qualifications. 
<LI class=text>Translation of disinfectant qualification results to cleaning procedures to prevent contamination. 
<LI class=text>Cleaning procedures-what should be addressed. 
<LI class=text>How to monitor efficacy of the cleaning program. 
<LI class=text>Examples of disinfectant validation successes will be discussed. 
<LI class=text>FDA observations related to Disinfection and Cleaning. </LI></UL>
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<TD class=text height=36><STRONG><STRONG><A class=style24 href="http://email.complianceonline.com/cgi-bin18/DM/t/hY3D0V3H340PrQ0rmV0Et" target=_blank><U>Click here to purchase</U></A><SPAN class=text1> (Use coupon code </SPAN></STRONG></STRONG><SPAN class=style25>115770</SPAN><STRONG><STRONG><SPAN class=text1>)</SPAN></STRONG></STRONG></TD>
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<P><SPAN class=style20><STRONG><STRONG>Who Will Benefit:</STRONG></STRONG></SPAN></P>
<P class=text>This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the Pharmaceutical, Biotech, and Medical Device fields.</P>
<UL>
<LI class=text>QA and QC Managers 
<LI class=text>Disinfectant Validation Managers 
<LI class=text>Operations Managers 
<LI class=text>Cleanroom Managers 
<LI class=text>Personnel and contractors that clean and disinfect cleanrooms 
<LI class=text>Regulatory Compliance Managers &amp; Environmental Monitoring Managers 
<LI class=text>Contract laboratories 
<LI class=text>Microbiologists 
<LI class=text>Manufacturing personnel 
<LI class=text>Validation and facilities personnel 
<LI class=text>Cleaning Contractors and in-house cleaning personnel </LI></UL></TD>
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<TD vAlign=center align=left height=44><SPAN class=style22><SPAN class=style20><B>Instructor Profile:</B></SPAN> </SPAN></TD>
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<TD vAlign=top align=left bgColor=#f4f4f4><A href="http://email.complianceonline.com/cgi-bin18/DM/t/hY3D0V3H340PrQ0rmW0Eu" target=_blank><IMG height=75 alt="Jim Polarine" src="http://www.complianceonline.com/images/products/medium/701767.jpg" width=60 border=0></A></TD>
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<TD class=text1 vAlign=top align=left width="85%"><STRONG>Jim Polarine</STRONG>, is a technical service specialist at STERIS Corporation. He has been with STERIS Corporation for over eight years, where his current technical focus is microbial control in Cleanrooms and other critical environments. He has lectured in North America, Europe, Asia, Latin America, and Puerto Rico on issues related to disinfection and sanitation in Cleanrooms. Mr. Polarine is a frequent industry speaker and has worked on several book article publications related to cleaning and disinfection and contamination control. He is currently co-authoring several articles and is an author on the PDA technical report on cleaning and disinfection. He is also currently active on the PDA task force on cleaning and
 disinfection. He has presented at key industry events for PDA, ISPE, AALAS, IVT, University of Tennessee, SWE, and Barnett International on cleaning and disinfection and contamination control. </TD>
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[Openflow-dev] Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated compan

[Openflow-dev] Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies