Informazione tecnica HSE / 25 ° anno
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Guidance on information requirements and chemical safety assessment
Version 1.0 August 2019
This document has two parts, the first addresses the findings of the ECHA/RAC – SCOEL Joint Task Force that examined alignment of methodologies for setting exposure limits at the workplace, whilst the second part outlines how to prepare a scientific report for identifying such exposure limits.
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Table of Contents
DOCUMENT HISTORY
Appendix R.8-17: Guidance for preparing a scientific report for health based exposure limits at the workplace
Part I. Alignment of methodologies in accordance with the ECHA/RAC-SCOEL Joint Task Force findings
Part II. How to prepare a scientific report for health based exposure limits at the workplace
A.8-17.1. Introduction
A.8-17.1.1 Regulatory process for setting limit values
A.8-17.2. Preparation of the report for the derivation of workplace exposure limit values
A.8-17.2.1 Data collection
A.8-17.2.2 Health effects
A.8-17.2.2.1. Evaluation of the hazard data and selection of points of departure
A.8-17.2.2.2. Specific considerations on health effects and Mode of Action
A.8-17.2.2.3. Outcome of the hazard assessment
A.8-17.2.3 Exposure limit values and notations
A.8-17.2.3.1. Occupational Exposure Limits
A.8-17.2.3.2. Short Term Exposure limits
A.8-17.2.3.3. Biological Limit Value
A.8-17.2.3.4. Biological Guidance Value
A.8-17.2.3.5. Notations
A.8-17.2.3.6. Cancer dose-response assessment
A.8-17.2.4 Methodological aspects of exposure monitoring
A.8-17.2.4.1. Air monitoring
A.8-17.2.4.2. Biological monitoring
References
Fonte: ECHA
Direttiva 2001/82/CE del Parlamento europeo e del Consiglio, del 6 novembre 2001, recante un codice comunitario relativo ai medicinali veterinari
(GU L 311, 28.11.2001)
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