December 5, 2024
Published by Joachim Nuyttens at December 5, 2024
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Deviations: Understanding OOS, OOT, and OOE in Pharmaceutical QC Laboratories

In the pharmaceutical and life sciences industries, product quality and patient safety are paramount. But what happens when processes don’t go according to plan? Managing deviations—unexpected events that diverge from approved standard operating procedures (SOPs), guidelines, or specifications—is crucial for maintaining compliance, quality, and safety throughout manufacturing, distribution, storage, and testing.  A deviation can occur when a parameter, measurement or analytical result exceeds a defined threshold, signalling a potential risk. Addressing these issues promptly and effectively is essential to prevent […]
December 2, 2024
Lab Technician evaluation environmental monitoring data
Published by Joachim Nuyttens at December 2, 2024
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Real-Time Environmental Monitoring: a Recent Innovation in Sterile Manufacturing

The pharmaceutical industry is undergoing a transformation, driven by the latest updates to GMP regulations like Eudralex Annex 1. This evolution demands more robust and efficient environmental monitoring solutions, particularly in the manufacturing of sterile medicinal products. One of the most promising advancements in this field is Real-Time Environmental Monitoring (RTEM), which provides continuous insights into air quality and contamination risks, ultimately enhancing compliance and operational efficiency.  The Need for Real-Time Monitoring  Traditionally, environmental monitoring (EM) has relied on growth-based methods, […]
October 14, 2024
QC lab hplc
Published by Harris Bui-Vandeput at October 14, 2024
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What is Quality Control (QC)

Quality Control (QC) is the department which ensures that the incoming materials, products, utilities and cleanrooms are of sufficient quality for their use. The importance of QC stems from the undeniable obligation to deliver quality product that guarantees patient safety. Therefore, the need of a QC department has been made compulsory by several regulations including the EudraLex’s guidelines for GMP and FDA’s 21 CFR.   As the name suggests, the quality of incoming material, products, cleanrooms and utilities is verified in […]
October 7, 2024
Root Cause Analysis
Published by Harris Bui-Vandeput at October 7, 2024
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Root Cause Analysis

In the pharmaceutical industry, quality isn’t just a goal—it’s a requirement. To meet the high standards of safety and effectiveness, companies must continually address and resolve any deviations, product defects, or unexpected issues that arise. Enter Root Cause Analysis (RCA)—a structured approach that digs deep to uncover the underlying cause behind these problems.  RCA is essential for several reasons. First and foremost, it protects patient safety. By identifying the root cause of deviations and other issues, companies can take the […]