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FDAnews Announces — Disinfectant Testing and Validation Webinar, June 29, 2017

Disinfectant Testing and Validation
**An FDAnews Webinar**
June 29, 2017 — 1:30 p.m. – 3:00 p.m. ET

Think of cleaning and disinfecting as personal oral hygiene. Manufacturers want (and need) their cleanrooms really clean. No bacteria, no molds, no spores, no harmful residue…nothing, or as close to “nothing” as humanly possible.

Distressingly, levels of bacterial and mold contamination are on the rise. The FDA and EMU have responded with growing numbers of warning letters, 483s and other sanctions. For drug, device, biologics and supplement makers — compounders too — keeping it clean gets harder every day.

What are the best products to use? In what combination? On what schedule? How to test? These are just some of the questions being asked everyday on this subject.

Take charge of contamination. Sign up today for an all-new webinar from FDAnews featuring Jim Polarine Jr. MA., a recognized expert on disinfectant testing and validation.

Mr. Polarine takes attendees on a deep dive into the specifics of cleanroom sanitation. In this fast-paced hour-and-a-half learning session, attendees will discover:

  •     Proven ways to limit cleanroom contamination from incoming items
  •     Proper cleanroom design and condition
  •     Best products to control bacterial and mold spores
  •     Current sporicide and disinfectant regulations in the U.S. and the E.U.
  •     Proven approaches to coupon testing and determining spore contamination sources
  •     And much more!

Attendees will learn ways to address even such resistant species as Bacillus cereus, and walk through case studies on testing intricacies including porosity of surfaces, surface sterilization, and pooling on surfaces.

One patient death can destroy a company. Avoid lawsuits and liability, and keep regulators at arm’s length. Learn how to keep cleanrooms cleaner.

Meet the Presenter:
Jim Polarine Jr. MA., Senior Technical Service Manager, STERIS Corp.

Mr. Polarine focuses on microbial control in cleanrooms and other critical environments. A frequent lecturer on cleaning and disinfection in cleanrooms, he co-chairs the microbial investigations task force of the Parenteral Drug Assn. (PDA) and was a co-author of PDA’s Technical Report #70 on Cleaning and Disinfection. In addition to the PDA, he is a member of SIMB, ISPE, IEST, ASM, ASTM, AAAS, AOAC and ACS. He previously worked as a clinical research coordinator with the Department of Veterans Affairs and as a biology and microbiology instructor at the University of Illinois.

Who Will Benefit:

  •     QA and QC Managers
  •     Disinfectant Validation Managers
  •     Operations Managers
  •     Cleanroom Managers
  •     Personnel and contractors who clean and disinfect cleanrooms
  •     EH&S Managers
  •     Regulatory Compliance Managers
  •     Environmental Monitoring Managers

Webinar Details:
Disinfectant Testing and Validation
**An FDAnews Webinar**
June 29, 2017 — 1:30 p.m. – 3:00 p.m. ET

$287 per site

Easy Ways to Register:
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

Read the full story at

Source: PRWeb
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