GUIDELINE TO:
Contamination Control in Pharmaceutical, Biotech, and Medical Device Clean rooms
February 22, 2010 WEBINAR
NOON - 1:30 pm EST
Registration fee shown below is for one (1) person. Call for group discounts.
Controlling a cleanroom environment is critical to get the best product yield. Do you know enough to avoid common mistakes that cost big bucks?
This Contamination-Control training will provide valuable assistance to companies that need to validate their cleaning and disinfection programs.
Fact: Cleanroom contamination can result in downtime and burgeoning production costs. The billion-dollar Hubble Space Telescope did not perform as designed because of a particle smaller than 0.5 microns.
This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs. The end user will get a complete overview of the basics of how to control the cleanroom environment and how to get the best possible product yield.
The basics of personnel practices, and cleaning and disinfection will be discussed. The most common source of contamination in the cleanroom is people; it is thus important to cover common mistakes in behavior and gowning. Facility design and conditions will be addressed as well since these are also a contributor to contamination.
Areas Covered in the seminar:
- Review the most common mistakes people make in cleanrooms that lead to contamination.
- Learn how to develop a successful contamination control program.
- Learn ways to improve facility design and maintenance.
Who will benefit:
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. The employees who will benefit include:
- QA and QC Managers
- Disinfectant Validation Managers
- Operations Managers
- Cleanroom Managers
- Personnel and contractors that clean and disinfect cleanrooms
- Regulatory Compliance Managers & Environmental Monitoring Managers
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: PRICED PER PERSON
$365 for one (1) person.
Call for group discounts for multiple participants at your company.
610-399-4897
ECCWEB162
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