(Q36249437)

13 August 2017

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title

The role of the benchmark dose in a regulatory context (English)

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13 August 2017

Kim Z Travis

1

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13 August 2017

Ian Pate

series ordinal

2

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13 August 2017

Zoe K Welsh

series ordinal

3

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13 August 2017

language of work or name

English

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publication date

6 September 2005

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Regulatory Toxicology and Pharmacology

13 August 2017

published in

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13 August 2017

volume

43

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13 August 2017

issue

3

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13 August 2017

page(s)

280-291

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Benchmark Dose Workshop: Criteria for Use of a Benchmark Dose to Estimate a Reference Dose

13 August 2017

cites work

1 reference

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Limitations to empirical extrapolation studies: the case of BMD ratios

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Estimating noncancer uncertainty factors: are ratios NOAELs informative?

7 January 2021

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Investigation of the potential impact of benchmark dose and pharmacokinetic modeling in noncancer risk assessment

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A new method for determining allowable daily intakes.

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Critical issues in benchmark calculations from continuous data

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Comparison of available benchmark dose softwares and models using trichloroethylene as a model substance

7 January 2021

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Quantalization of continuous data for benchmark dose estimation

7 January 2021

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Procedures for calculating benchmark doses for health risk assessment.

7 January 2021

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Evaluation of subchronic toxicity data using the benchmark dose approach

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Recognition of adverse and nonadverse effects in toxicity studies

7 January 2021

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A human health risk assessment of boron (boric acid and borax) in drinking water

7 January 2021

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Characterizing dose-response: I: Critical assessment of the benchmark dose concept

7 January 2021

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Benchmark calculations in risk assessment using continuous dose-response information: the influence of variance and the determination of a cut-off value.

7 January 2021

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Benchmark dose risk assessment for formaldehyde using airflow modeling and a single-compartment, DNA-protein cross-link dosimetry model to estimate human equivalent doses.

7 January 2021

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7 January 2021

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The benchmark approach applied to a 28-day toxicity study with Rhodorsil Silane in rats. the impact of increasing the number of dose groups

7 January 2021

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7 January 2021

Identifiers

DOI

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13 August 2017

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