On Demand

Combining Particle and Microbial Sensors to Fully Meet Regulatory Requirements

Monitoring of nonviable and viable particles in a cleanroom is critical to meet regulatory requirements. An environmental monitoring system effectively collects, manages, and reports on data from both types of sensors.

Total particle contamination is a mixture of nonviable and viable particles. Historically, nonviable particles are monitored continuously while viable particles have been monitored on a less frequent basis. In modern aseptic manufacturing, both types should be monitored continuously to obtain an accurate indication of the cleanroom’s condition.

An ideal monitoring program provides the sampling data required and ensures data integrity through the use of an automated system to track any changes. The system used to track and record data must meet the requirements of 21 CFR Part 11 and should be incorporated into an automated Environmental Monitoring System.

Download this webinar to learn how to meet regulatory contamination monitoring requirements.

What You Will Learn:

  • Key regulations related to Environmental Monitoring Systems.
  • How to incorporate particle and microbial sensors into an Environmental Monitoring System.
  • The types of data and reports that should be expected from an Environmental Monitoring System.
Webinar Presented By:
Paul Hartigan
Global Product Line Manager Instruments and Sensors

Paul Hartigan is the Global Product Line Manager for Instruments and Sensors with Particle Measuring Systems. He has held various product management responsibilities over the last 10 years with Particle Measuring Systems including responsibility for Liquids, Aerosol and Microbial based products along with Environmental Monitoring Systems software and hardware. Hi responsibilities have included developing the latest technologies into products for use in Life Science cleanroom operations. Paul holds a B.S. in Electrical Engineering and a Master’s degree in Business. He has written numerous papers related to the application of products in the Life Sciences industry and presented at organizations throughout the world, including instruction at various trade organizations.