Location: Philadelphia, PA

Cleaning Validation Conference
August 20 - 22, 2019

Join the STERIS Life Sciences team at the Cleaning Validation Conference in Philly! With three days of speakers and comprehensive sessions on all things cleaning validation from best practices to regulatory trends and risk-based approaches this is critical to cleaning processes and validation success.  


Don’t miss our expert, Beth Kroeger speaking at the show:


Regulatory Pulse - Emerging Regulations and Enforcement Trends in Cleaning and Mitigation of Cross Contamination 

Presented by Beth Kroeger, Technical Services Manager 

Wednesday, August 21 at 10:00 AM 


Throughout the cleaning validation lifecycle, it is important to review the process for any changes that may have occurred.  It is also important to monitor the process in an attempt to identify any differences or process drift between the validated process and the current state.  This review should be performed yearly with the product review and/or with the cleaning validation lifecycle review which ensures the operation is always in a state of control and audit preparedness. To ensure audit readiness, as it related to a validated cleaning process a facility should:



  • Understand current focus of FDA inspections by reviewing current findings from regulatory inspections and identify trends relevant to cleaning validation
  • Review any change controls that were issued which could impact the validated state or process
  • Verify that training programs and documentation adequately address the needs of a robust cleaning program

Click Here to Register