CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 60763 | LVS EN ISO 13408-1:2015 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | Atcelts |
| 23112 | LVS EN ISO 14937:2002 /AC:2004 | Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 35153 | LVS EN ISO 13408-6:2011 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005) | Atcelts |
| 37341 | LVS EN ISO 13408-6:2011/ A1:2013 | Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013) | Atcelts |
| 26001 | LVS EN 15424:2007 | Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and Formaldehyde | Atcelts |
| 35155 | LVS EN ISO 13408-2:2011 | Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003) | Atcelts |
| 32632 | LVS EN ISO 11137-2:2007 /AC:2009 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006/Cor 1:2009) | Atcelts |
| 35748 | LVS EN ISO 25424:2011 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) | Atcelts |
| 9305 | LVS EN ISO 17665-1:2006 | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 9311 | LVS EN ISO 11137-3:2006 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects | Atcelts |
Displaying 61-70 of 176 results.