10 % discount for validation of reprocessing of medical devices under GLP-conditions
The validation of reprocessing procedures for reusable medical devices according to ISO 17664-1 and -2 under GLP for the US-market is an important hot topic and key for registration of medical devices with FDA. Of course we can use the recently published frame standard ANSI/AAMI ST98:2022 as a basis but also the German guidelines, such as ISO 15883-series.
We are ready to market in our bactericidal laboratory as of July 1st 2023 to offer these services under GLP and subsequently FDA compliant. The 10 % discount will be granted for all quotations accepted from now on until the end of 2023.
Take a look inside our laboratory: