EPTIS
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Diagnostics of cervical cytology

[Méhnyakcitológia diagnosztikája]

EPTIS Ringversuch Nr. 1278491 | Letze Änderung 2026-03-19 | URL: https://www.eptis.bam.de/pts1278491 https://www.eptis.bam.de/pts1278491

Name des Anbieters
Name des Anbieters QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd. QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd.
Ansässig in Hungary
Sprache(n) English, Hungarian
Anmerkungen All smears are available for participants only in digital form. a. Conventional smear 5 healthy and abnormal conventional smears per survey from routine cytology cases, stained according to Papanicolaou. Evaluation according to the Bethesda 2014 classification system via QualiCont's online ’Pathology Program’. After the evaluation, it is possible to review the annotated smears from the reference laboratory on the QualiCont site. A Certificate of participation is issued by QualiCont. b. LBC (liquid based sample) ThinPrep smear 5 healthy and abnormal conventional LBC smears per survey from routine cytology cases, stained according to Papanicolaou. Evaluation according to the Bethesda 2014 classification system via QualiCont's online ’Pathology Program’. After the evaluation, it is possible to review the annotated smears from the reference laboratory on the QualiCont site. A Certificate of participation is issued by QualiCont. c. Conventional and LBC smear It is possible to evaluate both conventional and liquid-based (LBC) smears according to the practice of the laboratory. QualiCont has had accredited status as the QualiCont as a Proficiency Test Provider complies with the criteria of MSZ EN ISO/IEC 17043:2010 standard since 26 March 2014. The QualiCont has been accredited according to the MSZ EN ISO/IEC 17043:2023 standard since 18 December 2025. Our Company is a Proficiency Testing Provider Organisation accredited by NAH (National Accreditation Authority) under the NAH-8-0002/2023 registration number. As the result of the accreditation process performed by NAH, our Company has accredited status until 9 March 2028.
Klassifizierung
Produktgruppen Health care / medical devices
Human test material
Prüfgebiete Medical analysis
Technische Einzelheiten
Prüfobjekt Prüfeigenschaft Prüfmethode
Slides (see Remarks) Different staining methods (see Remarks)
Ringversuchsziele
Zielgruppe des Ringversuchs In vitro medical laboratories
Relevante Rechtsvorschriften oder Normen ISO 15189 – Medical laboratories – Requirements for quality and competence ISO/TS20658:2017 – Medical laboratories – Requirements for collection, transport, receipt and handling of samples VIM3 – Vocabulaire International de Métrologie WHO – Guidance on regulations for the Transport of Infectious Substances
Weitere Ziele validation of testing methods
Teilnehmerzahl
Anbieter unabhängig überprüft (akkreditiert, benannt, anerkannt)
Die Durchführung des Ringversuchs ist in Auftrag gegeben durch
Kosten
Teilnahmegebühr on demand
Regelmässig durchgeführt Ja (four times a year)
Der Ringversuch wird durchgeführt seit
Kontaktdaten des Anbieters
Anbieter Kontaktperson
QualiCont In Vitro Diagnostic Quality Control Nonprofit Ltd.
Feketesas u. 19-21. I/7
6720 Szeged
Hungary

Telefon: +36 30 462 5864
Fax:
Web: http://www.qualicont.com/qc/index_en.html http://www.qualicont.com/qc/index_en.html
Ms. Eszter Mezey
Telefon: +36 30 462 5864
Fax:
E-Mail: mail@qualicont.com mail@qualicont.com
Haben Sie einen Fehler entdeckt? Bitte wenden Sie sich an den zuständigen EPTIS Koordinator für Hungary, Ms Eszter Mezey. Ms Eszter Mezey.
Haben Sie Fragen? Senden Sie uns eine E-Mail: eptis@bam.de.
Anwendungsversion: 1.23-SNAPSHOT.20230502124635-7925ae379a631fc1ececff45d2921c8db38877d5