footnote__5
Risk assessment is generally carried out in four clearly defined stages with specific objectives in order to identify hazards, dose and risk relationships, and to measure the magnitude of exposure to determine the risk level and estimated impact on the exposed receptors:
← b) · All articles · a) →
Source: EUR-Lex (Cellar) · retrieved 2026-09-25 · Text as adopted (Official Journal); later amendments are not incorporated in this text.