Disinfectant efficacy testing is one of the most critical components in the pharmaceutical industry, particularly the surface…
Finding the out-of-Specification (OOS) results is one of the most stressful moments in a pharmaceutical quality control…
Sterility testing is one of the most sensitive microbiological tests performed in the pharmaceutical industry, and Fluid…
Sterile pharmaceutical products demand more than just a successful sterilization cycle. They require a holistic system of…
In pharmaceutical manufacturing, product release traditionally depends on finished product testing, especially sterility testing. However, for certain…
Documentation errors in pharma are the most common reasons for audit observations. These errors may occur even…
The USFDA audit process, also referred to as an FDA inspection, is a structured, risk-based, on-site examination…
Calibration in pharmaceuticals is one of the most fundamental activities in the industry. Every measurement we record—temperature,…
Setting up a pharmaceutical cleanroom is one of the most critical activities in the pharmaceutical industry. A…
Introduction Disinfectants in pharmaceutical cleanrooms play a vital role in controlling microbial contamination and ensuring that medicines…