Tuesday February 4, 2020
12:00 Noon – 1:00 pm EDT
Instructor: Jim Polarine
This seminar will cover the current industry regulations in the US, Europe and Globally related to cleaning and disinfection. Regulatory expectations will be covered including the latest revision of Annex I and recent FDA Warning Letters and 483’s related to cleaning and disinfection will be covered. The current antimicrobial products used in cleanroom industry will be discussed. Cleaning frequency, disinfectant rotation, rinsing and residue removal, disinfectant coverage calculations, and the most current equipment and methodologies for cleaning and discinfection will be covered in detail. The topic of sterility as it relates to cleanroom disinfectants and sporicides will be explained. This seminar will provide the audience with the ability to design and effective risk-based approach to cleaning and disinfection.
Areas Covered in the Seminar:
- Effective ways to rotate disinfectants
- The need to control bioburden involves a sound cleaning and disinfection program
- The most current industry methods for applying disinfectants
- Effective methods for controlling residues
- All the necessary components will be discussed that will allow end users to be in compliance with FDA and EMA
Who Will Benefit:
This webinar will provide valuable assistance to all FDA and EMA 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
- Operations Managers
- Cleanroom Managers
- Personnel and contractors that clean and disinfect cleanrooms
- EH&S Managers
- Regulatory Compliance Managers & Environmental Monitoring Managers
Fee:
$385 for one person
$700 2-5 people
$999 6-10 people
Questions? support@eccwebinars.com
ECC-161