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Medical laboratories

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  • Testing and calibration laboratories
  • Medical laboratories
  • Inspection bodies
  • Certification bodies of management systems
  • Certification bodies for persons
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  • Verifiers - EMAS
  • Verifiers - GHG
  • Good laboratory practice (GLP)
  • Accreditation of Proficiency Testing Providers
Published: 17.05.2021.
Updated: 31.03.2025.

General documents, including Application

Flexible scope accreditation (LATAK-D.041-05/03.2025)
LATAK Policy for the Metrological Traceability of Measurement Results (LATAK-D.034-07/07.2021)
LATAK Policy for Participation in Proficiency Testing Programmes and Interlaboratory Comparisons (LATAK-D.007-12/01.2025)
Accreditation scheme for conformity assessment of medical laboratories (LATAK - D.15189-2023/M/02/10.2024)
Accreditation scheme for conformity assessment of medical laboratories (LATAK - D.15189-2013/M/03/08.2023)
List of documents 15189:2013 (F.002.M-03)
List of documents 15189:2023 (F.002.M-05)
Information on the calibration status of equipment / benchmarks (F.060.00-02)
OVERVIEW OF INTERLABORATORY (EXTERNAL) COMPARISON (F.045)
LIST OF REFERENCE MATERIALS/ STANDARDS/ CALIBRATORS (F.046)
LIST OF PERSONNEL (IN THE FIELD OF COMPLIANCE ASSESSMENT) (F.059)

Accredited medical examinations assure that clinical laboratories focus on maintaining patients’ healthcare, directly connected with improved patient safety, risk mitigation and operational efficiency.

Accreditation to ISO 15189 also means that the laboratory meets the management system principles of ISO 9001.

Conformity assessment bodies shall apply also respective mandatory documents of the EA, ILAC and IAF. List of LATAK mandatory documents is described in LATAK D.008. EA, IAF and ILAC documents are listed in EA-INF/01 (see http://www.european-accreditation.org/publications)

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