- Validation of the effectiveness of antiseptics and disinfectants on all types of surfaces
- Validation of the effectiveness of intermediate and final cleaning processes
- Validation of cleaning and disinfection instructions for reusable instruments (ancillary) according to AAMI TIR: 12, AAMI TIR: 30, AAMI ST98, NF EN ISO 15883-1, NF EN ISO 15883-5, NF EN ISO 17664 and the FDA GUIDE (Reprocessing Medical Devices in Health Care Setting)
- Drafting of user manuals or Instructions For Use (IFU)
- Testing of antiseptics and disinfectants to European standards
