Toronto, Canada (PRWEB) October 03, 2013
Good Manufacturing Practice (GMP) requires manufacturers of finished bio/pharmaceutical products to effectively clean their facilities and equipment prior to production and disinfect regularly to ensure product safety.
The key to successful facility cleaning is understanding the complete process, including the unique differences between materials cleaning validation and disinfectant efficacy studies, how the two processes are related and the challenges associated with each.
During this presentation you will learn how to establish the best and most cost-effective approach to a cleaning, disinfection and monitoring program, including:
- Best practices for chemistry cleaning validation.
- Best practices for microbiology cleaning validation.
- Understanding the difference between cleaning validation and disinfectant studies and how they relate.
- Challenges and variables related to disinfection of surfaces. A Q&A with the audience will follow the main presentation.
For more information about this event or to register, visit: http://xtalks.com/cleaning-validations-and-disinfectant-studies.ashx.
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
To learn more about Xtalks visit http://xtalks.com/ContactUs.ashx.
Karen Lim (416) 977-6555 ext 227