With the revision of VDA 19.1 (2025), process-oriented monitoring of technical cleanliness is coming into focus much more strongly for the first time, alongside…
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…
Learn how the dry extraction method using suction in accordance with VDA 19.1 delivers reproducible results with a specially developed adaptation – ideal for…
What does this mean and what is the difference to validation of reprocessing according to the manufacturer's instructions? What analyses are typically carried…
