+Article 25 Human biomonitoring study
---+Article 25 1
---+Article 25 2

Article 25 Human biomonitoring study

1. Overview

Article 25 1

1. By 2 January 2030, the ECHA and the EFSA, in cooperation with the EEA, shall, in the context of the data generation mechanism referred to in Article 24, commission a Union-wide human biomonitoring study covering all Member States.

Article 25 2

2. Member States shall cooperate with the ECHA, the EFSA and the EEA in the planning and organisation of the human biomonitoring study and provide the necessary technical assistance and administrative support to the parties contracted by the ECHA or the EFSA to perform the sampling in order to enable sampling in their territories and to ensure that the samples are sufficiently representative. The human biomonitoring study shall comply with ethical and confidentiality standards.

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
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