octobre 5, 2025
Published by Joachim Nuyttens at octobre 5, 2025
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Présentation de Wouter et Ilke à l’ISPE

La semaine dernière, nos collègues Wouter Van Beylen et Ilke Diels ont fait une présentation lors de l’événement ISPE CQV and Emerging Leaders organisé sur le site de MSD Boxmeer, aux Pays-Bas. Ils ont partagé leur expertise sur la validation du nettoyage. Ce fut une excellente présentation devant une salle de conférence comble, confirmant l’expérience de Wouter et Ilke en matière de validation du nettoyage.
juin 12, 2025
Published by Joachim Nuyttens at juin 12, 2025
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Reflecting on The Past six Months: The Launch of Our HVAC / Testing Team

Since January, we have been proud to offer specialized services in HVAC and cleanroom testing. Our dedicated team of technicians and engineers is equipped to handle balancing, testing of HVAC installations, and commissioning and qualification activities for HVAC and cleanrooms, adhering to standards such as ISO 14644. As we approach the six-month mark, it’s a good time to reflect on this journey and our achievements. The Beginning In December 2024, we made the decision to launch our new team. With […]
décembre 5, 2024
Published by Joachim Nuyttens at décembre 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 […]
décembre 2, 2024
Lab Technician evaluation environmental monitoring data
Published by Joachim Nuyttens at décembre 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, […]
août 30, 2021
regulations compliance
Published by Joachim Nuyttens at août 30, 2021
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Audit trail requirements on GxP computerized systems

According to Wikipedia an audit trail is a chronological record providing documentary evidence of the sequence of activities that have affected at any time a specific operation, procedure, event, or device. The first uses of audit trails date back to ancient civilizations when rudimentary methods emerged to manage goods, soldiers and financial transactions. Audit trails to ensure data integrity came into the spotlight when US regulation 21CFR Part 11 was issued in 1997. Part 11 requires the use of secure, […]