+Article 6 3

Article 6 3

3.   The EEA shall process human biomonitoring data constituting personal data for the following purposes only:

(a)

assessing the impact of chemicals on human health and the environment;

(b)

monitoring time and spatial trends in exposure;

(c)

developing health risk and impact indicators;

(d)

monitoring the impact of regulatory intervention;

(e)

supporting regulatory risk assessments and regulatory risk management;

(f)

supporting policy making and the development of legislation;

(g)

facilitating the processing of human biomonitoring data by the Commission, the ECHA, the EFSA, the EMA, and EU-OSHA in accordance with paragraphs 4 to 8.

1. Overview

,
Summary Regulation

1.1 References

1.2 Identified Requirements

1.3 Related Standards

2. Identified Requirements

Requirements
Source Requirement

3. Related Standards

Standards
Source Requirement
  • Builddate: 12.12.2025 00:00:00 -Doknr: CELEX:32025R2455
  • EULAW -

    EN: Legal acts of the European Union from EUR-Lex, https://eur-lex.europa.eu/. © European Union. Re-use is authorised by Decision 2011/833/EU, provided the source is acknowledged; the consolidated texts are licensed under CC BY 4.0 (EUR-Lex legal notice). Divided into sections and converted into the GRCA format, the wording unchanged. Only the legislation published in the Official Journal of the European Union is deemed authentic.

    DE: Rechtsakte der Europäischen Union aus EUR-Lex, https://eur-lex.europa.eu/. © Europäische Union. Weiterverwendung nach Beschluss 2011/833/EU mit Quellenangabe gestattet; die konsolidierten Fassungen stehen unter CC BY 4.0 (Rechtlicher Hinweis von EUR-Lex). In Abschnitte aufgeteilt und in das GRCA-Format umgewandelt, der Wortlaut unverändert. Verbindlich sind allein die im Amtsblatt der Europäischen Union veröffentlichten Rechtsakte.