EN ISO 16638-1:2017

European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Symbols and abbreviated terms
5 Purpose and need for monitoring programmes
6 General aspects
7 Reference levels for uranium
8 Routine monitoring programmes
9 Special monitoring programmes
10 Task-related monitoring programmes
11 Performance criteria for laboratories
12 Quality assurance and quality control for bioassay
   laboratories
13 Procedure for the assessment of exposures
14 Reporting and documentation
Annex A (informative) - Nuclear data of U-238 and U-235
        decay
Annex B (informative) - Default classification of uranium
        compounds
Annex C (informative) - Measurement techniques for uranium
Annex D (informative) - Committed effective dose per unit intake
        for uranium compounds
Annex E (informative) - Estimation of uncertainties for internal dose
        assessments
Bibliography

ISO 16638-1:2015 specifies the minimum requirements for the design of professional programmes to monitor workers exposed to uranium compounds. It establishes principles for the development of compatible goals and requirements for monitoring programmes and dose assessment for workers occupationally exposed to internal contamination. It establishes procedures and assumptions for risk analysis, monitoring programmes and the standardised interpretation of monitoring data in order to achieve acceptable levels of reliability for uranium and its compounds. It sets limits for the applicability of the procedures in respect to dose levels above which more sophisticated methods have to be applied.Uranium is both radiologically and chemically toxic. Hence, the scientific bases of current occupational exposure standards are reviewed in addition to radiation exposure limits. This International Standard addresses those circumstances when exposure could be constrained by either radiological or chemical toxicity concerns.ISO 16638-1:2015 addresses, for uranium and its compounds, the following items:a) purposes of monitoring and monitoring programmes;b) description of the different categories of monitoring programmes;c) quantitative criteria for conducting monitoring programmes;d) suitable methods for monitoring and criteria for their selection;e) information that has to be collected for the design of a monitoring programme;f) general requirements for monitoring programmes (e.g. detection limits, tolerated uncertainties);g) frequencies of measurements;h) procedures for dose assessment based on reference levels for routine and special monitoring programmes;i) assumptions for the selection of dose-critical parameter values;j) criteria for determining the significance of monitoring results;k) interpretation of workplace monitoring results;l) uncertainties arising from dose assessment and interpretation of bioassays data;m) reporting/documentation;n) quality assurance;o) record keeping requirements.It is not applicable to the following items:a) monitoring of exposure due to uranium progeny, including radon;b) detailed descriptions of measuring methods and techniques for uranium;c) dosimetry for litigation cases;d) modelling for the improvement of internal dosimetry;e) potential influence of counter-measures (e.g. administration of chelating agents);f) investigation of the causes or implications of an exposure;g) dosimetry for ingestion exposures and for contaminated wounds.