EN ISO 15189:2022
(Main)Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
This document specifies requirements for quality and competence in medical laboratories.
This document is applicable to medical laboratories in developing their management systems and assessing their competence. It is also applicable for confirming or recognizing the competence of medical laboratories by laboratory users, regulatory authorities and accreditation bodies.
This document is also applicable to point-of-care testing (POCT).
NOTE International, national, or regional regulations or requirements can also apply to specific topics covered in this document.
Medizinische Laboratorien - Anforderungen an die Qualität und Kompetenz (ISO 15189:2022)
Dieses Dokument legt Anforderungen an die Qualität und Kompetenz in medizinischen Laboratorien fest.
Dieses Dokument ist anwendbar auf medizinische Laboratorien bei der Entwicklung von deren Management¬systemen und der Beurteilung ihrer Kompetenz. Des Weiteren ist es anwendbar bei der Bestätigung oder Anerkennung der Kompetenz medizinischer Laboratorien durch Kunden des Laboratoriums, Aufsichts¬behörden und Akkreditierungsstellen.
Dieses Dokument ist auch auf die patientennahe Sofortdiagnostik (POCT) anwendbar.
ANMERKUNG Internationale, nationale oder regionale Regelungen bzw. Anforderungen können ebenfalls für bestimmte Themen in diesem Dokument gelten.
Laboratoires de biologie médicale - Exigences concernant la qualité et la compétence (ISO 15189:2022)
Le présent document spécifie les exigences concernant la qualité et la compétence des laboratoires médicaux (laboratoires de biologie médicale et autres laboratoires médicaux comme les structures d’anatomie et de cytologie pathologiques).
Le présent document est également applicable aux laboratoires médicaux dans le cadre de l’élaboration de leur système de management et de l’évaluation de leur compétence. Il est également applicable par les utilisateurs des laboratoires, les autorités réglementaires et les organismes d’accréditation pour confirmer ou reconnaître la compétence des laboratoires médicaux.
Le présent document est applicable aux examens de biologie médicale délocalisée (EBMD).
NOTE Des réglementations ou exigences internationales, nationales ou régionales peuvent également s’appliquer à des sujets spécifiques traités dans le présent document.
Medicinski laboratoriji - Zahteve za kakovost in kompetentnost (ISO 15189:2022)
Ta dokument določa zahteve za kakovost in kompetentnost medicinskih laboratorijev.
Ta dokument uporabljajo laboratoriji pri oblikovanju sistemov upravljanja kakovosti in vrednotenju lastne kompetentnosti. Uporablja se tudi za potrjevanje ali prepoznavanje kompetentnosti medicinskih laboratorijev s strani laboratorijskih uporabnikov ter upravnih in akreditacijskih organov.
Ta dokument se uporablja tudi za testiranje ob pacientu (POCT).
OPOMBA: Za določene teme, ki so zajete v tem dokumentu, se lahko uporabljajo tudi mednarodni, nacionalni ali regionalni predpisi ali zahteve.
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 15189:2023
01-marec-2023
Nadomešča:
SIST EN ISO 15189:2013
SIST EN ISO 22870:2017
Medicinski laboratoriji - Zahteve za kakovost in kompetentnost (ISO 15189:2022)
Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
Medizinische Laboratorien - Anforderungen an die Qualität und Kompetenz (ISO
15189:2022)
Laboratoires de biologie médicale - Exigences concernant la qualité et la compétence
(ISO 15189:2022)
Ta slovenski standard je istoveten z: EN ISO 15189:2022
ICS:
03.120.10 Vodenje in zagotavljanje Quality management and
kakovosti quality assurance
11.100.01 Laboratorijska medicina na Laboratory medicine in
splošno general
SIST EN ISO 15189:2023 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 15189:2023
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SIST EN ISO 15189:2023
EN ISO 15189
EUROPEAN STANDARD
NORME EUROPÉENNE
December 2022
EUROPÄISCHE NORM
ICS 03.120.10; 11.100.01 Supersedes EN ISO 15189:2012, EN ISO 22870:2016
English Version
Medical laboratories - Requirements for quality and
competence (ISO 15189:2022)
Laboratoires de biologie médicale - Exigences Medizinische Laboratorien - Anforderungen an die
concernant la qualité et la compétence (ISO Qualität und Kompetenz (ISO 15189:2022)
15189:2022)
This European Standard was approved by CEN on 15 November 2022.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this
European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by
translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management
Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2022 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 15189:2022 E
worldwide for CEN national Members.
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SIST EN ISO 15189:2023
EN ISO 15189:2022 (E)
Contents Page
European foreword . 3
2
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SIST EN ISO 15189:2023
EN ISO 15189:2022 (E)
European foreword
This document (EN ISO 15189:2022) has been prepared by Technical Committee ISO/TC 212 "Clinical
laboratory testing and in vitro diagnostic test systems" in collaboration with Technical Committee
CEN/TC 140 “In vitro diagnostic medical devices” the secretariat of which is held by DIN.
This European Standard shall be given the status of a national standard, either by publication of an
identical text or by endorsement, at the latest by June 2023, and conflicting national standards shall be
withdrawn at the latest by December 2025.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 15189:2012 and EN ISO 22870:2016.
This document has been prepared under a Standardization Request given to CEN by the European
Commission and the European Free Trade Association.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria,
Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye
...
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