Location: Online

Disinfectant Validation & Efficacy Testing Webinar
September 11, 2019

12:00 - 1:00 PM EDT


Join us for our upcoming complimentary webinar on disinfection validation and efficacy testing.  Companies with controlled environments require aseptic processing of components and products. A validation cleaning and disinfection process is required to ensure these aseptic areas are consistently maintained. This webinar will cover how the United States Food and Drug Administration (FDA), the European Medicines Agency (EMA), the United Kingdom Medicines and Healthcare Products Regulatory Agency (MHRA) and Ireland’s Health Products Regulatory Authority (HPRA) evaluate these processes during cGMP inspections. Our team will also cover how to establish a cGMP compliant process and the required efficacy within the controlled environment. 


What we’ll cover:

  • Disinfectant Regulation and EPA Registration 
  • Label Claims and Testing 
  • Disinfectant Validation and Test Methods 
  • In vitro Testing Considerations 

Who will benefit: 

  • 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

Click Here to Register