Leveraging Microbial Contamination Monitoring Data for Actionable Insights to Meet and Exceed the Auditor’s Expectations
Effectively monitoring microbial contamination in your cleanroom has become even more essential over the last year, especially with the upcoming release of EU GMP Annex 1. Modern pharmaceutical manufacturers are already generating and managing big data from environmental monitoring; the next step is to create actionable insights and ensure 21CFR11 compliance. This webinar discusses data collection, 21CFR11 data management and the generation of actionable insights. We will review how this is accomplished by leveraging industry standards such as the FDA/ICH guidelines that encourage the use of control charts as statistical tools to guarantee that a manufacturing process remains in a state of control (the validated state).
Event : Free Webinar
Presenters: Paola Lazzeri ,Giulia Artalli
Date : 26 Feb 2020 at 10hh0
Pamas GMBH exhibitions in 2020
CONEXPO Las Vegas March 2020
SALON FORUM LABO Lyon March 2020
Analytica Munich March- April 2020
International conferences and exhibitions in Sorption Science 2020
SCI From Science to Shelf: Innovating through Formulation, 21 -22 Jan, London, UK.
NL Catalysis and Chemistry Conference, 4-6 March, Noordwijkerhout, NL.
German Zeolite Conference, 25- 27 March, Hanover, Germany.