What Makes a Good Environmental Monitoring System?

Reliably leveraging data to improve your process — that's the basis of any environmental monitoring system. Learn how TSI and TSI FMS Software make this goal a reality for our users everyday.

WHAT YOU WILL LEARN

• Difference between cleanroom classification (ISO 14644-1:2015 Part 1) and cleanroom monitoring (ISO 14644-2:2015 Part 2)
• How a facility monitoring system (FMS) can reduce risk and improve yield
• Key elements of a reliable facility monitoring system
• Advantages of real-time, continuous monitoring in Grade A and support environments
• Universal communication via OPC UA—transition to Pharma 4.0

Orginally held July 1, 2020.

RECORDING AVAILABLE

CLICK HERE to check out more webinars that are part of the TSI Pharmaceutical Manufacturing Webinar Series—highlighting the industry’s hottest topics.

ABOUT THE PRESENTERS

Simon Tebb is the EMEA Sales Manager at TSI. He has worked with TSI for over 14 years specializing in applications of particle measurement instrumentation in Europe, Middle East and Africa. Prior to joining TSI, Simon worked in the automotive industry in production engineering. He holds a Bachelor Honours Degree in Engineering from Sheffield Hallam University, U.K., and a Masters Degree in Business from the University of Wolverhampton, U.K.

Alain Nezer is a Senior Contamination Control Application Specialist at TSI GmbH. He has worked with TSI for over 6 years specializing in applications of particle measurement instrumentation in Europe, Middle East and Africa. Prior to joining TSI, Alain worked in the automotive industry in production engineering. He holds an Engineering Degree in Electronics from the Belgium Army. Alain has approximately 28 years of experience in the pharmaceutical industry, mainly in facility monitoring systems and particle counters.