90/679/EEC - Protection of workers from risks related to exposure to biological agents at work
Directive 90/679/EEC aims to protect workers from health and safety risks arising from exposure to biological agents at work. It establishes minimum requirements for employers to assess risks related to biological exposure, categorized into four risk groups based on severity and transmissibility. Employers must avoid the use of hazardous biological agents where possible, implement measures to prevent or reduce exposure, provide appropriate protective equipment and hygiene facilities, and ensure worker training and information. The directive mandates keeping records of workers exposed to high-risk agents and requires prior notification to authorities when using certain biological agents. Health surveillance is to be provided for at-risk workers, including access to medical records and relevant vaccinations. It also emphasizes consultation with workers and clear procedures for handling accidents or incidents involving biological agents. Overall, the directive integrates into broader EU occupational health and safety legislation to safeguard workers from infections, allergies, and toxic effects associated with biological agents in the workplace.
Purpose
Council Directive 90/679/EEC, adopted on 26 November 1990, aims to protect workers from health and safety risks related to exposure to biological agents at work. It establishes minimum provisions to prevent or reduce such risks in the workplace, ensuring safer working environments. This directive is the seventh individual directive under the framework of Directive 89/391/EEC ("Framework Directive") and applies alongside it, without prejudice to more specific or stringent rules.
The directive covers risks arising from biological agents that may provoke infections, allergies, or toxic effects and emphasizes the importance of risk assessment, preventive measures, and health surveillance to protect workers.
Key obligations
Risk Assessment and Control
- Employers must assess the nature, degree, and duration of workers’ exposure to biological agents, considering all groups of such agents present.
- Risk assessments must be updated regularly and when conditions change.
- Employers must provide information used in risk assessments to competent authorities upon request.
Risk Reduction and Prevention
- The use of harmful biological agents must be avoided or replaced with less dangerous ones when possible.
- Where risk cannot be eliminated, exposure must be reduced to the lowest level necessary through:
- Limiting the number of exposed workers.
- Designing work processes to minimize release of biological agents.
- Implementing collective and individual protection measures.
- Ensuring proper hygiene practices and warning signs.
- Establishing emergency plans for accidents involving high-risk agents.
- Testing for the presence of biological agents outside primary containment.
- Safe collection, storage, disposal, and transport of agents and contaminated waste.
Information and Training
- Workers must receive sufficient training and information regarding risks, preventive measures, hygiene requirements, protective equipment, and emergency procedures.
- Written instructions and displayed notices are required, particularly for serious accidents or handling of group 4 agents.
- Workers must immediately report incidents involving biological agents.
- Employers must communicate accident information promptly to workers and their representatives.
Worker Records and Notification
- Employers must keep lists of workers exposed to group 3 and 4 biological agents, recording details of exposure and any incidents. Records should be kept for 10 years or up to 40 years for agents causing persistent or latent infections.
- Prior notification is required to competent authorities before first use of group 2, 3 or 4 biological agents in the workplace.
- Notifications must be updated with significant changes affecting safety and health.
Health Surveillance
- Member States must arrange health surveillance for workers exposed to biological agents at risk.
- Surveillance should occur before exposure and periodically thereafter.
- Medical records of exposed workers must be kept for at least 10 years or longer for specific agents.
- Vaccinations should be offered to non-immune workers where appropriate.
- Health surveillance must enable implementation of protective measures and provide information to affected workers about the results.
Consultation and Participation
- Workers and their representatives must be consulted and involved in matters relevant to biological agent exposure and health protection measures.
Affected products and actors
- Biological agents: Micro-organisms (including genetically modified ones), cell cultures, human endoparasites, grouped into four risk categories from group 1 (low risk) to group 4 (high risk with serious community spread potential).
- Employers: Required to conduct risk assessments, implement protection measures, notify authorities, provide training, keep records, and comply with all obligations.
- Workers: Exposed or potentially exposed employees who must receive information, training, and protection; also responsible for reporting incidents.
- Health and Safety Authorities: Competent authorities receiving notifications, conducting oversight, and ensuring compliance.
- Health Surveillance Providers: Doctors or competent authorities responsible for health monitoring and advice.
Implementation timeline
- The directive applies from its date of adoption-26 November 1990.
- Prior notifications to competent authorities for use of biological agents must be given at least 30 days before beginning work.
- Risk assessments and protective measures must be continuously maintained and updated as required.
- Records related to exposure and health surveillance must be retained for periods specified (10 to 40 years) according to the nature of the biological agents involved.
- Member States have to implement the directive in accordance with their national laws and practices and ensure appropriate enforcement mechanisms are in place.
This directive sets a comprehensive framework to ensure worker protection from biological risks at workplaces involving exposure to potentially hazardous microorganisms and biological substances. It complements the broader Framework Directive 89/391/EEC and further directives concerning genetic modification and containment.
This Directive applies to all work activities in which workers are or may be exposed to biological agents that can cause infection, allergy, or toxicity. It covers micro-organisms, including genetically modified ones, cell cultures, and human endoparasites. The scope includes activities involving any of the four risk groups of biological agents, classified based on their potential to cause human disease and the availability of effective prophylaxis or treatment. Employers must assess and manage risks related to exposure through preventive and protective measures. The Directive is relevant to sectors and activities where biological agents are present or used, including laboratories, healthcare, biotechnology, agriculture, and waste management, ensuring worker safety through risk assessment, exposure prevention, health surveillance, and information dissemination. It excludes deliberate uses governed by other specific genetic modification directives.
Die Richtlinie 90/679/EWG schützt Arbeitnehmer vor Gefährdungen durch biologische Arbeitsstoffe am Arbeitsplatz. Sie legt Mindestanforderungen zur Vorbeugung und zum Gesundheitsschutz fest und differenziert biologische Arbeitsstoffe in vier Risikogruppen nach ihrem Gefährdungspotenzial. Arbeitgeber sind verpflichtet, Risiken durch Ermittlung, Abschätzung und technische bzw. organisatorische Maßnahmen, etwa durch Ersatz gefährlicher Arbeitsstoffe, Minimierung der Exposition und Hygienemaßnahmen, zu reduzieren. Zudem müssen Arbeitnehmer informiert, unterwiesen und bei Gefahrenschutzmaßnahmen beteiligt werden. Es besteht eine Meldepflicht gegenüber den Behörden, insbesondere bei biologischen Arbeitsstoffen höherer Risikogruppen. Ein Verzeichnis exponierter Arbeitnehmer ist zu führen und langfristig aufzubewahren. Auch bei Unfällen oder Zwischenfällen sind sofortige Melde- und Informationspflichten vorgesehen. Die Richtlinie stellt sicher, dass gesundheitliche Gefährdungen durch biologische Arbeitsstoffe systematisch minimiert werden und fördert so die Sicherheit und den Gesundheitsschutz der Beschäftigten in der EU.
Zweck
Die Richtlinie 90/679/EWG zielt auf den Schutz der Arbeitnehmer vor Gefährdungen durch biologische Arbeitsstoffe am Arbeitsplatz ab. Sie ist eine von mehreren Einzelrichtlinien nach der EU-Rahmenrichtlinie 89/391/EWG und legt spezifische Mindestvorschriften zum Arbeitsschutz fest. Ziel ist es, Gesundheitsrisiken durch Infektionen, Allergien oder toxische Wirkungen, die von Mikroorganismen, genetisch veränderten Mikroorganismen, Zellkulturen und Humanendoparasiten ausgehen, zu verhindern oder zu minimieren. Dabei sind sowohl Präventions- als auch Schutzmaßnahmen zu berücksichtigen. Die Richtlinie berücksichtigt hierbei unterschiedliche Risikogruppen der biologischen Arbeitsstoffe und gewährleistet, dass Arbeitnehmer vor Infektionen und anderen gesundheitlichen Folgen geschützt werden.
Wichtige Verpflichtungen
Risikobewertung: Arbeitgeber müssen alle Tätigkeiten erfassen, bei denen eine Exposition gegenüber biologischen Arbeitsstoffen möglich ist. Art, Ausmaß und Dauer der Exposition sind zu ermitteln und regelmäßig zu beurteilen, insbesondere bei geänderten Arbeitsbedingungen.
Risikominimierung: Wenn Risiken bestehen, muss die Exposition vermieden oder soweit wie möglich reduziert werden. Hierfür sind technische und organisatorische Schutzmaßnahmen einzuführen, einschließlich der Begrenzung exponierter Arbeitnehmer, Gestaltung der Arbeitsverfahren zur Minimierung der Freisetzung biologischer Arbeitsstoffe und Einsatz kollektiver oder persönlicher Schutzausrüstung.
Ersetzung: Bevorzugt sind biologische Arbeitsstoffe einzusetzen, die weniger gefährlich sind, sofern dies technisch möglich ist.
Unterrichtung und Schulung: Arbeitnehmer sind ausreichend über Gefahren, Schutzmaßnahmen, Hygienevorschriften, den Gebrauch von Schutzausrüstung sowie das Verhalten bei Unfällen zu informieren und zu unterweisen. Die Unterrichtung soll zu Beginn der Tätigkeit erfolgen und bei Gefahrenerkennung angepasst bzw. wiederholt werden.
Hygienemaßnahmen: Am Arbeitsplatz muss sichergestellt werden, dass keine Nahrungsmittelaufnahme in gefährdeten Bereichen erfolgt, Schutzkleidung bereitsteht, sanitäre Einrichtungen vorhanden sind und kontaminierte Kleidung ordnungsgemäß behandelt wird.
Dokumentation und Meldepflichten:
- Führung eines Verzeichnisses gefährdeter Arbeitnehmer (insbesondere bei Exposition gegenüber Risikogruppe 3 und 4), das mindestens 10 Jahre (in besonderen Fällen bis zu 40 Jahre) aufzubewahren ist.
- Anmeldung der erstmaligen Verwendung biologischer Arbeitsstoffe der Risikogruppen 2 bis 4 bei den zuständigen Behörden mindestens 30 Tage vor Beginn der Arbeiten.
- Umgehende Meldung von Unfällen oder Zwischenfällen mit möglicher Freisetzung gefährlicher biologischer Arbeitsstoffe.
- Bereitstellung aller sicherheitsrelevanten Informationen für zuständige Behörden und betroffene Arbeitnehmer.
Zugang zu Informationen: Arbeitnehmer und deren Vertreter haben Zugang zu personenbezogenen und allgemeinen Sicherheitsinformationen bezüglich der biologischen Arbeitsstoffe.
Mitwirkung der Arbeitnehmer: Die Richtlinie fordert die Einbindung der Arbeitnehmer oder ihrer Vertreter bei Sicherheits- und Gesundheitsschutzmaßnahmen.
Betroffene Produkte und Akteure
Biologische Arbeitsstoffe: Dazu zählen Mikroorganismen (einschließlich genetisch veränderter Mikroorganismen), Zellkulturen sowie Humanendoparasiten, die potenziell Infektionen, allergische oder toxische Wirkungen hervorrufen können. Diese werden in vier Risikogruppen eingeteilt (1 bis 4) nach dem Grad der Gesundheitsgefährdung.
Arbeitgeber: Sind verpflichtet, umfassende Schutzmaßnahmen umzusetzen, Arbeitnehmer zu unterweisen, Risiken zu bewerten und Behörden zu informieren.
Arbeitnehmer: Sind diejenigen, die beruflich mit biologischen Arbeitsstoffen in Kontakt kommen oder kommen könnten.
Zuständige Behörden: Überwachen die Einhaltung der Richtlinie, erhalten Meldungen, prüfen die Anmeldung biologischer Arbeitsstoffe und haben Zugang zu Verzeichnissen und Gesundheitsakten.
Sicherheitsfachkräfte und Betriebsärzte: Werden in die Bewertung und Überwachung des Gesundheitsschutzes einbezogen.
Umsetzungszeitraum
Die Richtlinie 90/679/EWG wurde am 26. November 1990 verabschiedet. Die Mitgliedstaaten der Europäischen Union sind verpflichtet, sie in nationales Recht umzusetzen und dabei sicherzustellen, dass die darin enthaltenen Mindestanforderungen an Arbeitsschutzmaßnahmen eingehalten werden. Die genaue Frist zur Umsetzung ist in der originalen Richtlinie definiert (üblicherweise innerhalb von 2 Jahren), um eine rechtzeitige Anwendung und Anpassung nationaler Vorschriften zu gewährleisten.
Diese Richtlinie bildet eine wichtige Grundlage für den Schutz von Arbeitnehmern in Berufen, die mit biologischen Gefahrenstoffen zu tun haben, und harmonisiert Mindeststandards innerhalb der EU. Die Umsetzung trägt zum sicheren europäischen Arbeitsmarkt bei und schützt die Gesundheit der Arbeitnehmer nachhaltig.
Die Richtlinie 90/679/EWG gilt für Tätigkeiten, bei denen Arbeitnehmer im Rahmen ihrer beruflichen Tätigkeit biologischen Arbeitsstoffen ausgesetzt sein können. Biologische Arbeitsstoffe umfassen Mikroorganismen, einschließlich genetisch veränderter Mikroorganismen, Zellkulturen und Humanendoparasiten, die Infektionen, Allergien oder toxische Wirkungen hervorrufen können. Die Richtlinie findet Anwendung auf alle Branchen und Sektoren, in denen eine Exposition gegenüber solchen biologischen Arbeitsstoffen möglich ist, etwa in der Gesundheitsversorgung, Forschung, Landwirtschaft oder Industrie. Dabei wird das Risiko anhand der Art, des Ausmaßes und der Dauer der Exposition bewertet. Explizit sind biologische Arbeitsstoffe nach ihrem Infektionsrisiko in vier Risikogruppen unterteilt, von denen die Richtlinie insbesondere Schutzmaßnahmen bis zu und inklusive der gefährlichsten Gruppen umfasst. Die Richtlinie erstreckt sich auf alle Maßnahmen zum Schutz der Arbeitnehmer, die durch Exposition bei der Arbeit gegenüber diesen biologischen Arbeitsstoffen gefährdet sind.
La directive 90/679/CEE vise à protéger la santé et la sécurité des travailleurs exposés à des agents biologiques au travail. Elle impose des prescriptions minimales fondées sur l’évaluation des risques liés à ces agents, classés en quatre groupes selon leur dangerosité. Elle s’applique aux activités professionnelles où une exposition réelle ou potentielle aux agents biologiques existe. Les employeurs doivent évaluer les risques, éviter l’utilisation d’agents dangereux quand c’est possible, ou réduire l’exposition par des mesures techniques, organisationnelles et d’hygiène. Ils ont l’obligation d’informer et former les travailleurs, de fournir des équipements de protection, et de tenir une liste des travailleurs exposés aux agents des groupes 3 et 4, ainsi que de notifier les autorités compétentes avant la première utilisation de ces agents. Cette directive s’inscrit dans le cadre plus large de la directive 89/391/CEE sur la sécurité au travail, tout en tenant compte des évolutions technologiques et des risques spécifiques liés aux agents biologiques, afin d’assurer une meilleure protection sanitaire et contribuer à l’amélioration des conditions de travail dans l’Union européenne.
Objet
La directive 90/679/CEE vise à protéger la santé et la sécurité des travailleurs exposés à des agents biologiques dans le cadre de leur activité professionnelle. Elle fixe des prescriptions minimales pour prévenir les risques liés à cette exposition, en complétant la directive cadre 89/391/CEE relative à la sécurité et à la santé au travail. Elle s’applique sans préjudice de directives spécifiques relatives aux micro-organismes génétiquement modifiés.
Obligations principales
Évaluation des risques : L’employeur doit identifier, évaluer et, si nécessaire, réévaluer régulièrement la nature, le degré et la durée de l’exposition à des agents biologiques (article 3). Cette évaluation sert à déterminer les mesures de prévention et de protection nécessaires.
Substitution : Lorsque cela est possible, l’employeur doit remplacer un agent biologique dangereux par un agent moins dangereux ou non dangereux (article 5).
Réduction des risques : Si un risque est identifié, l’exposition doit être évitée ou, si ce n’est pas possible techniquement, réduite à un niveau sûr via des mesures telles que la limitation du nombre de travailleurs exposés, la conception sécurisée des processus, la protection collective et individuelle, l’hygiène et la gestion sécurisée des déchets (article 6).
Information aux autorités compétentes : L’employeur doit fournir, à la demande, des informations sur l’évaluation des risques, les mesures prises, les travailleurs concernés et les plans d’urgence en cas d’accident (article 7).
Mesures d’hygiène et protections individuelles : Fourniture de vêtements et équipements de protection appropriés, installation de sanitaires adaptés, règles strictes d’utilisation et de nettoyage des équipements de protection, interdiction de manger et boire dans les zones à risque (article 8).
Formation et information des travailleurs : Formation initiale et continue sur les risques, les précautions, les mesures d’hygiène et les comportements à adopter en cas d’incident (articles 9 et 10).
Gestion des données des travailleurs exposés : Tenue d’une liste des travailleurs exposés aux agents biologiques des groupes 3 et 4, conservée pendant au moins 10 ans, voire jusqu’à 40 ans selon le risque infectieux (article 11).
Consultation des travailleurs : Les représentants du personnel doivent être consultés concernant les mesures liées aux agents biologiques conformément à la directive cadre 89/391/CEE (article 12).
Notification préalable : L’utilisation initiale d’agents biologiques des groupes 2, 3 et 4 doit être notifiée aux autorités compétentes au moins 30 jours avant le début des travaux (article 13).
Produits et acteurs concernés
Agents biologiques : Micro-organismes, cultures cellulaires et endoparasites humains susceptibles de provoquer infection, allergie ou intoxication. Ces agents sont classés en quatre groupes de risque selon leur dangerosité pour l’homme (du groupe 1 non dangereux au groupe 4 hautement dangereux).
Employeurs : Tous ceux dont les activités exposent les travailleurs à ces agents biologiques.
Travailleurs : Ceux exposés ou susceptibles de l’être, qui bénéficient de la protection et de l’information prévues.
Autorités compétentes : Destinataires des informations et notifications, chargées du contrôle et du suivi.
Calendrier de mise en œuvre
La directive est d’application immédiate à compter de sa date de publication, avec des obligations en continu :
Évaluation des risques dès l’identification d’une activité impliquant des agents biologiques.
Notification préalable obligatoire au moins 30 jours avant la première utilisation d’agents biologiques des groupes 2, 3 ou 4.
Conservation des listes des travailleurs exposés : au minimum 10 ans après la fin de l’exposition, pouvant aller jusqu’à 40 ans selon le risque.
La formation et l’information doivent être assurées à l’embauche, puis régulièrement mises à jour.
Les employeurs doivent adapter les mesures en fonction de l’évolution technologique et des nouvelles connaissances sur les risques biologiques.
Cette directive constitue un cadre de prévention essentiel dans le domaine de la santé au travail, contribuant à la réduction des risques liés aux agents biologiques pour les travailleurs dans l’Union européenne.
La directive 90/679/CEE s'applique aux activités professionnelles dans lesquelles les travailleurs sont exposés ou risquent d'être exposés à des agents biologiques susceptibles de provoquer une infection, une allergie ou une intoxication. Elle couvre notamment les micro-organismes, y compris les micro-organismes génétiquement modifiés, les cultures cellulaires et les endoparasites humains. Le champ d’application comprend les secteurs et activités susceptibles d'impliquer une exposition à ces agents biologiques, notamment ceux classés en quatre groupes selon leur dangerosité. La directive vise à protéger la santé et la sécurité des travailleurs en établissant des prescriptions minimales spécifiques, en complément des règles générales de la directive 89/391/CEE. Elle s’applique sans préjudice des directives spécifiques relatives à l’utilisation confinée ou à la dissémination d’organismes génétiquement modifiés dans l’environnement.
General Information
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It sets the specific performance criteria for class II BSC for work with biological agents and specifies test procedures with respect to protection of the worker, the environment and product protection including cross-contamination.
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This document gives requirements and recommendations for installation, commissioning and routine testing of BSC.
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The requirements for the different classes are given in the respective parts of prEN 12469.
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This European Standard gives biological, physical and procedural containment measures for work with genetically modified plants including plants where the transferred genetic material is derived from a non-plant source. It defines measures to minimize hazards identified by risk analysis.
Containment may be provided in a greenhouse or in a growthroom, laboratory or other containment facility.
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This European Standard specifies performance criteria for valves used in biotechnological processes with respect to the potential risks to the worker and the environment from microorganisms in use. This European Standard applies where the intended use of the valve includes hazardous or potentially hazardous microorganisms used in biotechnological processes or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard10 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for piping and instrumentation used in biotechnological processes with respect to the potential risks to the worker and the environment from microorganisms in use. This European Standard applies where the intended use of the equipment includes hazardous or potentially hazardous microorganisms used in biotechnological processes or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard13 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for couplings used in biotechnological processes with respect to the potential risks to the worker and the environment from microorganisms in use. This European Standard applies where the intended use of the coupling includes hazardous or potentially hazardous microorganisms used in biotechnological processes or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard9 pagesEnglish languagee-Library read for1 day
This European Standard specifies basic requirements for microbiological safety cabinets (MSCs) with respect to safety and hygiene. This European Standard sets the minimum performance criteria for safety cabinets for work with microorganisms and specifies test procedures for microbiological safety cabinets with respect to protection of the worker and the environment, product protection and cross contamination. Mechanical, electrical, chemical or radioactive safety precautions are not covered in the standard but are covered in EN 610101-1, EN 292-1 and EN 292-2 (see Bibliography (1), (2) and (3)).
- Standard45 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for off-gas systems used in biotechnological processes with respect to the potential risks of microorganisms in use for the worker and the environment. This European Standard applies where the intended use of the off-gas system includes hazardous or potentially hazardous microorganisms used in biotechnological processes and/or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard16 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for filter elements and filtration assemblies used in biotechnological processes with respect to the potential risks of microorganisms in use for the worker and the environment. This European Standard applies where the intended use of the filter elements or filtration assemblies includes hazardous or potentially hazardous microorganisms used in biotechnological processes and/or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard19 pagesEnglish languagee-Library read for1 day
This European Standard specifies basic requirements for microbiological safety cabinets (MSCs) with respect to safety and hygiene. This European Standard sets the minimum performance criteria for safety cabinets for work with microorganisms and specifies test procedures for microbiological safety cabinets with respect to protection of the worker and the environment, product protection and cross contamination. Mechanical, electrical, chemical or radioactive safety precautions are not covered in the standard but are covered in EN 610101-1, EN 292-1 and EN 292-2 (see Bibliography (1), (2) and (3)).
- Standard45 pagesEnglish languagee-Library read for1 day
This European Standard gives guidance to the manufacturer of sampling and inoculation devices on providing instructions in the manufacturer's documentation accompanying his products in accordance with prEN 13312-3. It has the purpose of pointing out to him, which hazards can occur during operation, s so that he can take these into account in an adequate way during construction and will be in a positive to formulate information for use giving adequate consideration of safety...
- Standard13 pagesEnglish languagee-Library read for1 day
This European Standard gives guidance to the manufacturer of sampling and inoculation devices on providing instructions in the manufacturer's documentation accompanying his products in accordance with prEN 13312-3. It has the purpose of pointing out to him, which hazards can occur during operation, s so that he can take these into account in an adequate way during construction and will be in a positive to formulate information for use giving adequate consideration of safety...
- Standard13 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for off-gas systems used in biotechnological processes with respect to the potential risks of microorganisms in use for the worker and the environment. This European Standard applies where the intended use of the off-gas system includes hazardous or potentially hazardous microorganisms used in biotechnological processes and/or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard16 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for filter elements and filtration assemblies used in biotechnological processes with respect to the potential risks of microorganisms in use for the worker and the environment. This European Standard applies where the intended use of the filter elements or filtration assemblies includes hazardous or potentially hazardous microorganisms used in biotechnological processes and/or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard19 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for cell disrupters used in the biotechnological processes with respect to the potential risks of microorganisms in use for the worker or the environment. This European Standard applies where the intended use of the cell disrupter includes hazardous or potentially hazardous microorganisms used in biotechnological processes and/or where exposure of the worker or the environment to such microorganisms is restricted for reasons of safety.
- Standard13 pagesEnglish languagee-Library read for1 day
This European Standard provides guidance for factors and criteria considered by the experimenter for the valid design, execution and evaluation of an analysis of the molecular stability of the genomic modification with respect to life cycle, heritability and external factors. It describes the steps in the characterization of a GMO that should be followed to ensure the validity of the analysis of the molecular stability of the genomic modification. The type of molecular stability analysis is dependent on the objectives of the experiment.
- Standard16 pagesEnglish languagee-Library read for1 day
This European Standard gives guidance on methods for handling, inactivating and testing of waste containing organisms arising from biotechnology laboratory activities and processes. It is concerned with methods to reduce the risks arising from exposure to waste derived from laboratory-scale activities which contains organisms hazardous or potentially hazardous to humans, animals, plants or the environment.
- Standard21 pagesEnglish languagee-Library read for1 day
This European Standard specifies design requirements for plant buildings used for the safe handling of microorganisms and the product itself if it presents a biohazard. Note 1: When applying this European Standard, attention is drawn to the existing national regulations such as regulations concerning genetic engineering, water and environmental emission concerning the design requirements.
- Standard16 pagesEnglish languagee-Library read for1 day
This European Standard specifies minimum physical requirements for biological safety for laboratories at four reference physical containment levels which are appropriate for handling microorganisms of different risk groups. This European Standard primarily addresses the containment of microorganisms which can present a risk to human health. It applies to microbiology laboratories where the handling of microorganisms in bacteriology, mycology, virology, parasitology and/or genetic modification is carried out.
- Standard22 pagesEnglish languagee-Library read for1 day
This European Standard, in order to protect the worker and/or the environment, gives guidance on minimum physical biosafety measures for the containment of animals deliberately inoculated with microorganisms, including genetically modified microorganisms, which can present a risk to human or animal health or the environment. This European Standard does not apply to the containment of animals which have not been deliberately inoculated with microorganisms.
- Standard15 pagesEnglish languagee-Library read for1 day
This European Standard provides guidance for a quality control procedure of a diagnostic kit to assure that the assay results will fulfil the intended purpose of the test by both manufacturers and users. This European Standard applies to diagnostic kits used in agriculture, plant and animal pest and disease control monitoring of feed and environmental contamination due to microorganisms.
- Standard9 pagesEnglish languagee-Library read for1 day
This European Standard specifies performance criteria for pumps used in biotechnological processes, in which the release of microorganisms should be limited or prevented for reasons of safety. This standard applies if the intended use of the pump includes hazardous or potentially hazardous microorganisms. This standard applies to pumps with no auxiliary equipment, bordered by the connections on the unit of equipment. It also applies to pump systems equipped with all necessary auxiliary equipment necessary for operation of pumps and to accomplish cleaning and sterilization.
- Standard13 pagesEnglish languagee-Library read for1 day
This European Standard provides guidance concerning the procedures for setting up a valid sampling strategy to meet the objectives of a monitoring strategy for GMMs released into the environment. Since monitoring methods of microorganisms in environmental samples usually require pretreatment of the samples, for example the extraction and isolation of GMMs and/or their nucleic acid, this is included in scope of this European Standard. The sampling is to provide material to which subsequent analytical or biological methods for monitoring of GMMs can be applied.
- Standard12 pagesEnglish languagee-Library read for1 day
This European Standard gives guidance on the assessment and the selection of procedures for treatment of waste process microorganisms from biotechnological plant to ensure the safety of people and environment. This European Standard applies to wastes and effluents (solid, liquid and gaseous) emitted from biotechnological processes which include traditional processes such as brewing or food processing, fermentation of pharmaceutical and chemical products as well as biotechnological processes for environmental and agricultural application.
- Standard18 pagesEnglish languagee-Library read for1 day
Frequently Asked Questions
An EU Directive is a legislative act of the European Union that sets out goals that all EU member states must achieve. However, it is up to each member state to devise their own laws on how to reach these goals through national transposition. Directives are used to harmonize laws across the EU, particularly for the functioning of the single market.
Directive 90/679/EEC covers "Protection of workers from risks related to exposure to biological agents at work". There are 106 standards associated with this directive.
Harmonized standards under 90/679/EEC are European standards (ENs) developed by CEN, CENELEC, or ETSI in response to a mandate from the European Commission. When these standards are cited in the Official Journal of the European Union, products manufactured in conformity with them benefit from a presumption of conformity with the essential requirements of 90/679/EEC, facilitating CE marking and free movement within the European Economic Area.