Menu
0
Total price
0 €
PRICES include / exclude VAT
Homepage>BS EN ISO 13304-2:2022 Radiological protection. Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation ex vivo human tooth enamel dosimetry
sklademVydáno: 2023-03-13
BS EN ISO 13304-2:2022 Radiological protection. Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation ex vivo human tooth enamel dosimetry

BS EN ISO 13304-2:2022

Radiological protection. Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation ex vivo human tooth enamel dosimetry

Format
Availability
Price and currency
Anglicky Secure PDF
Immediate download
298.85 €
You can read the standard for 1 hour. More information in the category: E-reading
Reading the standard
for 1 hour
29.89 €
You can read the standard for 24 hours. More information in the category: E-reading
Reading the standard
for 24 hours
89.66 €
Anglicky Hardcopy
In stock
298.85 €
Označení normy:BS EN ISO 13304-2:2022
Počet stran:34
Vydáno:2023-03-13
ISBN:978 0 539 22961 5
Status:Standard
DESCRIPTION

BS EN ISO 13304-2:2022


This standard BS EN ISO 13304-2:2022 Radiological protection. Minimum criteria for electron paramagnetic resonance (EPR) spectroscopy for retrospective dosimetry of ionizing radiation is classified in these ICS categories:
  • 17.240 Radiation measurements
  • 13.280 Radiation protection
The purpose of this document is to provide minimum criteria required for quality assurance and quality control, evaluation of the performance and to facilitate the comparison of measurements related to absorbed dose estimation obtained in different laboratories applying ex vivo X-band EPR spectroscopy with human tooth enamel. This document covers the determination of absorbed dose in tooth enamel (hydroxyapatite). It does not cover the calculation of dose to organs or to the body. This document addresses: a) responsibilities of the customer and laboratory; b) confidentiality and ethical considerations; c) laboratory safety requirements; d) the measurement apparatus; e) preparation of samples; f) measurement of samples and EPR signal evaluation; g) calibration of EPR dose response; h) dose uncertainty and performance test; i) quality assurance and control.