This 90-minute webinar on personnel practices and microbial control in Pharmaceutical, Biotech, and Medical Device manufacturing will cover effective ways to train personnel on gowning and personnel practices in cleanroom operations to limit contamination. This webinar will also address controlling microorganisms on process equipment and product contact surfaces.
Why Should You Attend:
Training on personnel practices and microbial control on process equipment are a critical part of your facility operations and overall control program to meet FDA, EMA, IMB, and MHRA regulations. This process involves personnel training and having a sound cleaning and disinfection program to control microbes on process equipment surfaces in the cleanroom operation.
This 90-minute presentation will cover all the necessary components that will allow end users to be in compliance with FDA, MHRA, IMB, and EMA.
Areas Covered in the Seminar:
Conducting audits of personnel practices.
Using proper gowning and apparel.
Addressing bioburden and cleaning and sanitization or process equipment.
Discussing the most current methods for applying disinfectants, sanitizers, and sporicides on process equipment and in the cleanroom.
The need to control bioburden involves a sound cleaning and disinfection program.
Effective methods for controlling residues.
All the necessary components will be discussed that will allow end users to be in compliance with FDA and EMEA.
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
Added by complianceonlinecom on November 7, 2012