The Continuous Monitoring Concept for Pharmaceutical Manufacturing
In this webinar, we’ll dive deep into the continuous monitoring approach, suggested by the guidelines to monitor the aseptic process int the New Annex 1, published in August 2022.
Portable Particle Counting and Meeting GMP Annex 1
This webinar will review how portable particle counters are an essential tool to meet and exceed the latest requirements of GMP Annex 1 in your manufacturing process.
Data Integration Excellence: Benefits of Dedicated Cleanroom Monitoring Systems
In this webinar, we will explore the advantages of implementing customized Environmental Monitoring Systems (EMS) in your pharmaceutical facility.
Annex 1 Environmental Monitoring Common Questions and Answers
Environmental Monitoring expert Mark Hallworth shares questions he frequently receives, along with practical answers to help you meet your EM needs.
Webinar: Annex 1 Questions & Answers
Attend this interactive webinar to get answers to common questions, learn what the auditors will be expecting and how to meet those expectations.
New Technologies and Options for Real-Time Aerosol Particle Monitoring Within Semiconductor Process Tools
In this free webinar you’ll learn: 1) New possibilities for contamination control from the latest particle counting solutions, 2) How to leverage real-time particle data to troubleshoot problems and improve overall tool cleanliness, and 3) The benefits of achieving complete tool coverage using a multipoint manifold system.
WEBINAR: Data Analysis Techniques for Understanding Particle Contamination in High Purity Liquids
This webinar covers a range of useful data analysis techniques that may be applied to data from liquid particle counters.
Validation and Qualification Approach Outlined in New Annex 1 Revision
In this free webinar you’ll learn: 1) why validation and qualification are important in the pharmaceutical process, and 2) how to to implement the best practices required by GMP’s.
WEBINAR: Measurements in Compressed Air (ISO 8573 Standard Series)
This webinar shows you what you should consider when qualifying compressed air and what options are available for qualification. We also take a look at the classification of pharmaceutical gases according to ISO 8573-1.
WEBINAR: Characterization of Critical Factors Affecting the Stabilization Time of Particle Measurements in Ultra-Pure Water Systems
In this free webinar you’ll learn: 1) how long the liquid particle counter takes to clean up, and 2) how long it takes for the unit to report stable data in ultra-pure water systems.
