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
