AAMI - 11137-3
Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects
inactive
| Organization: | AAMI |
| Publication Date: | 1 January 2006 |
| Status: | inactive |
| Page Count: | 31 |
scope:
This part of ISO 11137 gives guidance on the requirements in ISO 11137 parts 1 and 2 relating to dosimetry. Dosimetry procedures related to the development, validation and routine control of a radiation sterilization process are described.
Document History
January 1, 2017
Sterilization of health care products—Radiation—Part 3: Guidance on dosimetric aspects of development, validation and routine control
This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
January 1, 2017
Sterilization of health care products-Radiation-Part 3: Guidance on dosimetric aspects of development, validation and routine
This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
11137-3
January 1, 2006
Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects
This part of ISO 11137 gives guidance on the requirements in ISO 11137 parts 1 and 2 relating to dosimetry. Dosimetry procedures related to the development, validation and routine control of a...
January 1, 2006
Sterilization of health care products—Radiation—Part 3: Guidance on dosimetric aspects
This part of ISO 11137 gives guidance on the requirements in ISO 11137 parts 1 and 2 relating to dosimetry. Dosimetry procedures related to the development, validation and routine control of a...
January 1, 2004
STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 3: GUIDANCE ON DOSIMETRIC ASPECTS OF DEVELOPMENT, VALIDATION AND ROUTINE
A description is not available for this item.
Related Products
Searching for related products...