Why Attend?
Attend this webinar to learn how to meet regulatory contamination monitoring requirements for your cleanroom.
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 current aseptic manufacturing, both types must be monitored continuously to obtain an accurate indication of the cleanroom's condition.
An effective monitoring program provides the required data 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 must be used.
Presented by
Paul Hartigan,
Global Product Line Manager Systems and Software
Paul Hartigan is the Global Product Line Manager for Software and Systems 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, with his latest role being involved in the Environmental Monitoring Systems.
