The human element can never be completely eliminated, but what can be done to mitigate errors and maintain your data's integrity?

Our upcoming webinar will discuss how utilizing an organized, risk-based approach to closing gaps in processes caused by human error allows users to demonstrate that data generated to prove product quality is integral and accurate. We'll also provide examples of how the industry can evaluate its own processes for unnecessary risks as well as how automation will increasingly play an important role in reducing a laboratory's risk for human error and data integrity violations.

Have a scheduling conflict?

Sign up even if you can't make it, we'll share the recording after.

Matthew provides technical expertise that enables customers to implement innovative rapid microbial solutions for endotoxin testing, identification, and detection. He earned his MBA in Six Sigma/Quality Management and uses that experience to drive to the root causes of complex QC and manufacturing problems. Matthew is also responsible for leading multiple teams specializing in cross-functional investigation, method development and validation, and beta testing for complex laboratory instrumentation.