42 C.F.R. PART 82--METHODS FOR CONDUCTING DOSE RECONSTRUCTION UNDER THE ENERGY EMPLOYEES OCCUPATIONAL ILLNESS COMPENSATION PROGRAM ACT OF 2000
TITLE 42--Public Health
CHAPTER I--PUBLIC HEALTH SERVICE, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER G--OCCUPATIONAL SAFETY AND HEALTH RESEARCH AND RELATED ACTIVITIES
PART 82--METHODS FOR CONDUCTING DOSE RECONSTRUCTION UNDER THE ENERGY EMPLOYEES OCCUPATIONAL ILLNESS COMPENSATION PROGRAM ACT OF 2000
Subpart A--INTRODUCTION
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Background information on this part.
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What is the purpose of this part?
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What are the basics of dose reconstruction?
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What Are the Requirements for Dose Reconstruction Under EEOICPA?
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How Will DOL Use the Results of the NIOSH Dose Reconstructions?
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Subpart B--DEFINITIONS
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Definition of terms used in this part.
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Subpart C--DOSE RECONSTRUCTION PROCESS
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Overview of the dose reconstruction process.
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For which claims under EEOICPA will NIOSH conduct a dose reconstruction?
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Will it be possible to conduct dose reconstructions for all claims?
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What sources of information may be used for dose reconstructions?
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What types of information could be used in dose reconstructions?
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How will NIOSH evaluate the completeness and adequacy of individual monitoring data?
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How will NIOSH add to monitoring data to remedy limitations of individual monitoring and missed dose?
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What types of information could be used to supplement or substitute for individual monitoring data?
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How will NIOSH calculate internal dose to the primary cancer site(s)?
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How will NIOSH address uncertainty about dose levels?
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Subpart D--REPORTING AND REVIEW OF DOSE RECONSTRUCTION RESULTS
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When will NIOSH report dose reconstruction results, and to whom?
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How will NIOSH report dose reconstruction results?
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How can claimants obtain reviews of their NIOSH dose reconstruction results by NIOSH?
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Who can review NIOSH dose reconstruction files on individual claimants?
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Subpart E--UPDATING THE SCIENTIFIC ELEMENTS UNDERLYING DOSE RECONSTRUCTIONS
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How will NIOSH inform the public of any plans to change scientific elements underlying the dose reconstruction process to maintain methods reasonably current with scientific progress?
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How can the public recommend changes to scientific elements underlying the dose reconstruction process?
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How will NIOSH make changes in scientific elements underlying the dose reconstruction process, based on scientific progress?
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How will NIOSH inform the public of changes to the scientific elements underlying the dose reconstruction process?
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