Sign up for this webinar to understand contamination, to prevent the problem from arising.
Our speaker will discuss sampling and testing methods for each of these specifications
Compressor 4.4 system requirements iso#
This subject will also be under discussion, and attendees will be presented with a compilation of FDA/GMP Guides, USP/EP as well as ISO air standards. For each, our speaker will discuss its cause and effect, and prevention strategies.įor validation and system monitoring purposes, you need to regularly test compressed air quality according to international standards. These are: solid particulate, water content, total oil content, and microbial bioburden. There are four main sources of contamination, which will be discussed during the webinar. It will also include component functions, and recommendations for optimal component types. You will obtain a detailed description of a typical pharmaceutical compressed air system, which points out its individual components and includes engineering schematics. However, to prevent contamination from occurring, you need to first understand the different types of contamination commonly found in compressed air, and how you can prevent your system from getting affected by them.ĭuring this webinar, our expert speaker will walk you through the subject, furnishing information which will help you perform your duties better. It is very important to have a good compressed air system in place, to ensure a contamination-free product. This ensures a strong quality system that keeps contamination at bay.Ĭompressed air can cause clean room and product contamination, but people often overlook this possibility. As such, it is important that the compressed air system used is designed, constructed and monitored well.
Compressed air is considered a crucial service in pharmaceutical use, as most of its applications involve direct contact with the product.
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