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GUIDELINE TO:
Designing and Implementing an Effective Cleaning
and Disinfection Program
August 27, 2009
WEBINAR
NOON - 1:30 pm EDT
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.
- Manufacturer’s regulations
- 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: $345 for one person.
Call for
special discounts for multiple participants from your company.
610-399-4897
ECC121
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