In this free webinar, learn how cleaning validation inefficiencies silently undermine overall equipment effectiveness (OEE), and how to fix them. Attendees will learn how capabilities like part-level ...
The industry needs a single standard cleaning limit at 25 mg/m2. At home, when washing the dishes, do we ever consider what meal they will be used for next? When plates and cutlery are taken out of ...
A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals. It is now possible, as demonstrated by Janssen (1), for drug ...
Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...
The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...
In 2021, the Pharmaceutical Cleaning Validation market was estimated to be worth approximately US$ 15.7 billion. With a predicted CAGR of 6.8% over the next ten years, the market is expected to be ...
This practical 1-day course covers basic issues in cleaning processes in pharmaceutical manufacturing, and the validation of those processes. After an introduction to the overall objectives, the ...
This is a practical based course. We explore the issues and pitfalls you may experience when performing Cleaning Validation. Help, guidance and training is given on techniques to overcome the issues ...
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