Slide background
Slide background




Guida UE: Monitoraggio biologico sul luogo di lavoro

ID 23819 | | Visite: 2054 | Documenti Sicurezza UEPermalink: https://www.certifico.com/id/23819

Guida EU Monitoraggio biologico sul luogo di lavoro

Guida UE: Monitoraggio biologico sul luogo di lavoro / 2025

ID 23819 | 15.04.2025 / In allegato (EN)

Monitoraggio biologico sul luogo di lavoro: orientamenti per gli esperti in materia di SSL e i luoghi di lavoro

Il biomonitoraggio occupazionale è uno strumento per la valutazione dell’esposizione alle sostanze chimiche sul luogo di lavoro.

La presente guida stabilisce principi comuni e illustra il ruolo e l’uso dei valori guida per il monitoraggio biologico e dei valori limite biologici.

Offre ai professionisti della sicurezza e della salute sul lavoro e ai dirigenti informazioni su come istituire e gestire un programma di biomonitoraggio e utilizzare i risultati per migliorare la prevenzione. Il documento approfondisce le questioni etiche per proteggere la riservatezza e i diritti dei lavoratori e offre a costoro informazioni su cosa aspettarsi da questo tipo di monitoraggio.

________

BIOLOGICAL MONITORING AT WORK: GUIDANCE FOR OSH EXPERTS AND WORKPLACES

BIOLOGICAL MONITORING AT WORK GUIDANCE FOR OSH EXPERTS AND WORKPLACES

This guide is for occupational hygienists, occupational health (and safety) professionals and managers who are considering setting up and/or managing a biomonitoring programme for chemical exposure in the workplace. It may also be helpful to worker representatives and health and safety representatives. It was developed by the European Agency for Safety and Health at Work (EU-OSHA) on request of the European Commission and sets out common principles for occupational biomonitoring.1 However, it is important that users check the national occupational safety and health (OSH) legislation that applies to them, which may be more detailed or stringent.

The guide is based on national and international guidance documents that are listed in the references section. It gives practical advice on setting up a programme and how to protect workers’ rights, explains what EU legislation says and the role and use of biological monitoring guidance values and biological limit values, and provides information on how occupational biomonitoring is to be used to improve prevention at workplaces rather than for research purposes or development of biological monitoring methodologies. There may be more detailed guidance available at the national or sectoral level. It is therefore recommended to check for any national regulations, standards or guidance that detail the national requirements.

Since biomonitoring involves measurements on biological samples collected from individuals, it is essential that the rights of the individual providing the sample are safeguarded. The guide explains how to set up an effective biomonitoring programme in the workplace context while protecting the rights of individual participants.

The guide covers the use of biomonitoring for exposures to chemicals in the workplace for the purposes of exposure assessment and health surveillance, including in case of accidents and chemical spillage. It is not intended to give detailed advice on its use in other areas, for example, overdose research or pre-employment screening and environmental surveys. However, some of the principles and technical information are common to these other uses.

...

Table of Contents

Introduction
Definitions
Health surveillance
Biological monitoring/biomonitoring
Biological limit value
Biological guidance value
Background
Relation to air monitoring
Criteria for the application of biomonitoring
Conclusions drawn from biological monitoring
Ethical issues
Consent
Requirements on those who carry out health surveillance and biological monitoring
How to set up a biomonitoring programme
Information for employers who want to set up a biomonitoring programme
Defining the purpose of biomonitoring
Consultation on the programme with workers or their representatives
Discussing and agreeing on the programme with the individual workers concerned
Managing a workplace biomonitoring programme
Who should be subjected to biomonitoring?
Selection of biomonitoring methods
Choice of test parameter
Sampling
Quality assurance
What elements must be taken into consideration to interpret the results of occupational biomonitoring?
Biomonitoring for prevention
Action in case of a health problem or exceedance of a BLV
Health surveillance and biomonitoring after the end of exposure
Record-keeping
Individual records
Collective results
Information about biomonitoring results to the concerned parties
Worker information
Information to the employer
Costs
Information for workers
When do I need health surveillance including biomonitoring?
Who carries out biomonitoring and monitors my health?
Who pays for biomonitoring or health surveillance?
What is a biomonitoring report and what is in it?
Do I have to undergo health surveillance and biomonitoring?
References

ANNEX 1
Choice of test parameter

...

Fonte: EU-OSHA

Collegati

Descrizione Livello Dimensione Downloads
Allegato riservato Guida UE Monitoraggio biologico sul luogo di lavoro.pdf
EU-OSHA 15.04.2025
839 kB 207

Tags: Sicurezza lavoro Rischio chimico Abbonati Sicurezza

Articoli correlati

Ultimi archiviati Chemicals

Lug 03, 2025 23

Regolamento (Euratom) 2021/765

Regolamento (Euratom) 2021/765 ID 24219 | 03.07.2025 Regolamento (Euratom) 2021/765 del Consiglio del 10 maggio 2021 che istituisce il programma di ricerca e formazione della Comunità europea dell'energia atomica per il periodo 2021-2025 che integra il programma quadro di ricerca e innovazione… Leggi tutto
Lug 03, 2025 19

Regolamento (Euratom) 2025/1304

 Regolamento (Euratom) 2025/1304 ID 24218 | 03.07.2025 Regolamento (Euratom) 2025/1304 del Consiglio, del 23 giugno 2025, che istituisce il programma di ricerca e formazione della Comunità europea dell’energia atomica per il periodo 2026-2027 che integra il programma quadro di ricerca e innovazione… Leggi tutto
ECHA compendium of analytical methods
Giu 27, 2025 344

ECHA compendium of analytical methods for enforcing REACH restrictions - Ed. 3.0 2025

ECHA compendium of analytical methods for enforcing REACH restrictions - Ed. 3.0 2025 ID 24178 | 27.06.2025 / Attached ECHA has updated its compendium of analytical methods to help authorities to enforce and companies to comply with REACH restrictions. The compendium consists of a collection of… Leggi tutto
ECHA 2025   Key Areas of Regulatory Challenge
Giu 11, 2025 860

ECHA 2025 - Key Areas of Regulatory Challenge

ECHA 2025 - Key Areas of Regulatory Challenge ID 24098 | 11.06.2025 / Attached The report introduces new topics to reflect ECHA’s growing responsibilities. It also covers emerging topics in waste and recycling that aim to support circularity and enhance Europe’s industrial competitiveness. For… Leggi tutto
REACH Authorisation List
Giu 09, 2025 856

REACH Authorisation Decisions List / Last update: 23.05.2025

REACH Authorisation Decisions List / Last update: 23.05.2025 ID 24091 | Last update: 09.06.2025 REACH Authorisation Decisions List of authorisation decisions adopted on the basis of Article 64 of Regulation (EC) No 1907/2006 (REACH). The list also includes reference to related documentation… Leggi tutto
In situ generated active substances and their products
Giu 07, 2025 925

In situ generated active substances and their products

In situ generated active substances and their products / ECHA Aprile 2025 ID 24087 | 07.06.2025 / Version 2 April 2025 Information requirements and risk assessment for approval and authorisation Recommendations of the BPC Working Groups.________ Il presente documento ha lo scopo di assistere gli… Leggi tutto
Giu 06, 2025 1069

Rettifica regolamento (UE) 2023/2055 - 06.06.2025

Rettifica regolamento (UE) 2023/2055 - 06.06.2025 ID 24080 | 06.06.2025 Rettifica del regolamento (UE) 2023/2055 della Commissione, del 25 settembre 2023, recante modifica dell’allegato XVII del regolamento (CE) n. 1907/2006 del Parlamento europeo e del Consiglio concernente la registrazione, la… Leggi tutto

Più letti Chemicals

Notifica HACCP
Apr 05, 2022 103081

Notifica ai fini registrazione Regolamento CE n. 852/2004

Notifica ai fini della registrazione (Reg. CE n. 852/2004) - Ex notifica sanitaria alimentare ID 7901 | 06.03.2019 / Modello notifica allegato [panel]Regolamento (CE) 852/2004...Articolo 6 Controlli ufficiali, registrazione e riconoscimento 1. Gli operatori del settore alimentare collaborano con le… Leggi tutto