What Is The Microbiology Of Air In Regulatory Manufacturing Environments?
Learn about the microbiology of the air, its importance and which airborne microbes can contaminate GMP manufacturing environments.
Learn about the microbiology of the air, its importance and which airborne microbes can contaminate GMP manufacturing environments.
Learn how to perform USP 1072 disinfectant challenge testing for cleaning validations to ensure your medical device or product meets FDA guidelines.
Learn how to determine the activity of a disinfectant and select an appropriate disinfectant for cleaning validations of manufacturing environments.
Learn about water sampling and when to use these methods for environmental monitoring of your parenteral products.
Learn the differences between aseptic and non-aseptic processes and which is the best one to use for your medical device or product.
Learn how to set up and run media fill simulations for aseptic process validations, when should it be performed and its importance for aseptic products.
Learn the differences between package integrity testing and environmental monitoring, and how these regulatory tests relate to medical devices and products.
Learn about airborne microbial samplings and how to test for environmental monitoring of aseptic manufacturing of your medical devices and products.