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ISO 13304-1:2013

Withdrawn
Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

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withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Radiological protection Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation Part 1: General principles
Available format(s)

Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users

Withdrawn date

22-07-2020

Language(s)

French, English

Published date

15-07-2013

The primary purpose of ISO 13304-1:2013 is to provide minimum acceptable criteria required to establish procedure of retrospective dosimetry by electron paramagnetic resonance spectroscopy and to report the results.

The second purpose is to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories.

ISO 13304-1:2013 covers the determination of absorbed dose in the measured material. It does not cover the calculation of dose to organs or to the body. It covers measurements in both biological and inanimate samples, and specifically:

  1. based on inanimate environmental materials, usually made at X-band microwave frequencies (8 GHz to 12 GHz);
  2. in vitro tooth enamel using concentrated enamel in a sample tube, usually employing X-band frequency, but higher frequencies are also being considered;
  3. in vivo tooth dosimetry, currently using L-band (1 GHz to 2 GHz), but higher frequencies are also being considered;
  4. in vitro nail dosimetry using nail clippings measured principally at X-band, but higher frequencies are also being considered;
  5. in vivo nail dosimetry with the measurements made at X-band on the intact finger or toe;
  6. in vitro measurements of bone, usually employing X-band frequency, but higher frequencies are also being considered.

For the biological samples, the in vitro measurements are carried out in samples after their removal from the person and under laboratory conditions, whereas the measurements in vivo may take place under field conditions.

NOTE The dose referred to in ISO 13304-1:2013 is the absorbed dose of ionizing radiation in the measured materials.

DevelopmentNote
Supersedes ISO/DIS 13304-1. (07/2013)
DocumentType
Standard
Pages
20
PublisherName
International Organization for Standardization
Status
Withdrawn
SupersededBy

Standards Relationship
NF ISO 13304-1 : 2013 Identical

ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories
ISO/IEC 17000:2004 Conformity assessment Vocabulary and general principles
ISO/IEC Guide 43-1:1997 Proficiency testing by interlaboratory comparisons Part 1: Development and operation of proficiency testing schemes
ISO/IEC 17011:2004 Conformity assessment General requirements for accreditation bodies accrediting conformity assessment bodies
ISO 9001:2015 Quality management systems — Requirements
ISO 9000:2015 Quality management systems — Fundamentals and vocabulary
ISO/IEC Guide 43-2:1997 Proficiency testing by interlaboratory comparisons Part 2: Selection and use of proficiency testing schemes by laboratory accreditation bodies
ISO/IEC Guide 98-3:2008 Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995)

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