Location: Online

Join the STERIS Life Sciences team for a wonderful learning opportunity during our upcoming webinar

Pharmaceutical, biotechnology and medical device companies often have controlled environments that require aseptic processing of components and products. To ensure that these aseptic areas are consistently maintained, a validated cleaning and disinfection process is required by regulatory authorities. The United States Food and Drug Administration (FDA), the European Medicines Agency (EMA), the United Kingdom Medicines and Healthcare Products Regulatory Agency (MHRA) & Ireland’s Health Products Regulatory Authority (HPRA) evaluate these processes during cGMP (current good manufacturing practice) inspections. Establishment of a cGMP compliant process requires that the disinfectants used are effective and demonstrate the required efficacy within their specific controlled environments. 

This Webinar Will Focus On: 
• 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

Time: 1:00 PM EDT
Duration: 90 min