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Life cycle testing is a crucial part of the approval process for medical devices. It ensures that products function safely and reliably throughout their entire…

Standards and regulations, risk assessment, testing methods

With the C|PS³flex, CleanControlling presents the latest generation of suction extraction systems for determining technical cleanliness in accordance with the…

What is the significance of volume flow measurement and which parameters must be observed?

Learn how the dry extraction method using suction in accordance with VDA 19.1 delivers reproducible results with a specially developed adaptation – ideal for…

Neuentwicklung: Multifunktionale Volumenstromanzeige zur kontinuierlichen Überwachung des Volumenstroms | Einfache Nachrüstung bestehender Systeme | Kompatibel…

Here you will find answers to frequently asked questions about accreditation in accordance with DIN EN ISO/IEC 17025 and ZLG recognition.

What does this mean and what is the difference to validation of reprocessing according to the manufacturer's instructions? What analyses are typically carried…

In this white paper, we look at ionic residues on electronic assemblies and their determination using the ROSE test and its application.