With the revision of VDA 19.1 (2026), process-oriented monitoring of technical cleanliness is coming into focus much more strongly for the first time, alongside…
Learn how the dry extraction method using suction in accordance with VDA 19.1 delivers reproducible results with a specially developed adaptation – ideal for…
Although endotoxins can pose a relevant risk to patient safety, they are not included in the ISO 10993 classification system for the biological evaluation of…
We are pleased to announce that CleanControlling will be the official distribution partner for BIDAG particles and reference standards in the future. This…
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…
