GUIDELINE TO:
Designing and Implementing an Effective Cleaning and Disinfection Program
May 21, 2010 WEBINAR
12:00 - 1:30 pm EST
Registration fee below is for one dial-in, one (1) person. Call for discounts to register more than one person
This webinar will cover the topic of "designing and implementing an effective cleaning and disinfection program," and will bring clarity to the cleaning and disinfection process by covering industry trends, regulatory expectations, and essential elements needed to keep the cleanroom in control. Regulatory expectations of FDA and EMEA inspectors will be discussed.
You will learn how to choose and apply cleaners and disinfectants properly depending on the surface, environment and product, which will reduce labor costs and commodity usage. Multiple laboratory segments to complement the lectures include sanitization of a Class 100/10,000 pharmaceutical cleanroom, proper equipment cleaning/disinfection procedures, and validation of disinfectant performance and application. In the end, you will be able to develop validation protocols and a proper cleaning and disinfection program to suit the needs of your company
In this webinar you wil learn:
I. How to ensure your cleaning and disinfection program is robust
• Learn disinfectant regulations.
o Manufacturer’s regulations
o Pharmaceutical and Biotech regulations
• Review “real world” examples of cleaning and disinfection programs.
• Increase awareness of elements that make cleaning and disinfection successful.
II. Troubleshooting problems related to cleaning and disinfection.
• Problems associated with contact time.
• Problems associated with dilution rates.
• Problems associated with application.
• Problems associated with corrosion or the porosity of substrates
III. Safety related to application and application techniques of disinfectants
• Safety of the concentrated disinfectant vs the use dilution
• Application of disinfectant products in cleanrooms and controlled areas
• Frequency of application will be addressed
IV. The elements of a successful disinfectant validation
• Regulations surrounding disinfectant validation
• Testing required for disinfectant validation.
I nstructor: Jim Polarine
Mr. Polarine is a technical service specialist at STERIS Corporation. He has been with STERIS Corporation for over nine 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 cleaning and disinfection in cleanrooms. Mr. Polarine is a frequent industry speaker and has worked on several books and 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 is part of the faculty at the University of Tennessee Parenteral Medication course. He has presented at key industry events for PDA, ISPE, AALAS, IVT, University of Tennessee, on cleaning and disinfection and contamination control. Mr. Polarine also frequently presents global industry webinars on Cleaning and Disinfection. Mr. Polarine graduated from the University of Illinois with a Master of Arts in Biology, and is a member of the PDA, ISPE, IEST, ASM, AALAS, ASTM, AAAS, AOAC, and ACS. He previously worked as a clinical research coordinator with the Department of Veteran’s Affairs and as a biology and microbiology instructor at the University of Illinois. His main hobby is storm chasing and is very active in tornado research and tornado safety
FEE: ONE DIAL-IN, ONE PERSON
$365 for one (1) person.
Call for group discounts for multiple participants at your company.
610-399-4897
ECCWEB183
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