Presenter: Dr Lise Vanderkelen (Department Head Micro & Pharma Services Nelson Labs Europe)
Reprocessing validations of Reusable medical devices have been overlooked for quite some time. But the upcoming MDR requirements and US FDA Scrutiny over reusable medical devices has shed a light to their importance and significance. The presentation will highlight some of the key aspects of what is required for validation studies for these type of devices and how to perform these validations. During her presentation, Lise Vanderkelen mainly focuses on cleaning validation for reusable devices. This presentation was recorded on 05 March at our Open House event.
