![Annex 1](https://www.pmeasuring.com/wp-content/uploads/2022/08/New-Annex-Image-1.jpg)
Environmental Monitoring According to Annex 1:2023
This post will explore the technicalities and practical applications of these guidelines, exploring its implications for cleanroom operations and microbial monitoring.
This post will explore the technicalities and practical applications of these guidelines, exploring its implications for cleanroom operations and microbial monitoring.
The most recent revision to USP 797 brings forth changes that touch various aspects of pharmaceutical practices. Here, we explore the USP Regulatory Standards Development Process.
This blog post discusses navigating choices in cleanroom viable air monitoring, offering fundamental insights to guide your approach.
Welcome to our USP 1116 questions and answers blog, where Particle Measuring Systems answers commonly asked questions pertaining to the USP 1116 guidance. What guidance is there for non-sterile facilities in regards to CRR (aseptic processing)? It is important to note that <1116> is a “general information” chapter, and as such,…