On Demand Webinar Archives

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.

Webinar

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.

Webinar Type: On Demand Webinar

Data Analysis Techniques for Understanding Particle Contamination in High Purity Liquids

Validation and Qualification Approach Outlined in New Annex 1 Revision

Measurements in Compressed Air (ISO 8573 Standard Series)

Characterization of Critical Factors Affecting the Stabilization Time of Particle Measurements in Ultra-Pure Water Systems

Without measurement there is no control®

Data Analysis Techniques for Understanding Particle Contamination in High Purity Liquids

Validation and Qualification Approach Outlined in New Annex 1 Revision

Measurements in Compressed Air (ISO 8573 Standard Series)

Characterization of Critical Factors Affecting the Stabilization Time of Particle Measurements in Ultra-Pure Water Systems

Get the latest updates, insights, and resources straight to your inbox

Without measurement there is no control®