Federal (United States) · Regulations
Subpart C — Dose Reconstruction Process
10 sections
10 sections
- 42 C.F.R. § 82.10Overview of the dose reconstruction process.
- 42 C.F.R. § 82.11For which claims under EEOICPA will NIOSH conduct a dose reconstruction?
- 42 C.F.R. § 82.12Will it be possible to conduct dose reconstructions for all claims?
- 42 C.F.R. § 82.13What sources of information may be used for dose reconstructions?
- 42 C.F.R. § 82.14What types of information could be used in dose reconstructions?
- 42 C.F.R. § 82.15How will NIOSH evaluate the completeness and adequacy of individual monitoring data?
- 42 C.F.R. § 82.16How will NIOSH add to monitoring data to remedy limitations of individual monitoring and missed dose?
- 42 C.F.R. § 82.17What types of information could be used to supplement or substitute for individual monitoring data?
- 42 C.F.R. § 82.18How will NIOSH calculate internal dose to the primary cancer site(s)?
- 42 C.F.R. § 82.19How will NIOSH address uncertainty about dose levels?