Title 42

PART 82 SUBPART C

Subpart C - Dose Reconstruction Process

• 42 U.S.C. 7384n(d) and (e); E.O. 13179, 65 FR 77487, 3 CFR, 2000 Comp., p. 321.
• 67 FR 22330, May 2, 2002, unless otherwise noted.

42:1.0.1.7.65.3.15.1	SECTION 82.10	82.10 Overview of the dose reconstruction process.
42:1.0.1.7.65.3.15.2	SECTION 82.11	82.11 For which claims under EEOICPA will NIOSH conduct a dose reconstruction
42:1.0.1.7.65.3.15.3	SECTION 82.12	82.12 Will it be possible to conduct dose reconstructions for all claims
42:1.0.1.7.65.3.15.4	SECTION 82.13	82.13 What sources of information may be used for dose reconstructions
42:1.0.1.7.65.3.15.5	SECTION 82.14	82.14 What types of information could be used in dose reconstructions
42:1.0.1.7.65.3.15.6	SECTION 82.15	82.15 How will NIOSH evaluate the completeness and adequacy of individual monitoring data
42:1.0.1.7.65.3.15.7	SECTION 82.16	82.16 How will NIOSH add to monitoring data to remedy limitations of individual monitoring and missed dose
42:1.0.1.7.65.3.15.8	SECTION 82.17	82.17 What types of information could be used to supplement or substitute for individual monitoring data
42:1.0.1.7.65.3.15.9	SECTION 82.18	82.18 How will NIOSH calculate internal dose to the primary cancer site(s)
42:1.0.1.7.65.3.15.10	SECTION 82.19	82.19 How will NIOSH address uncertainty about dose levels

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