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
