All Stories

  1. An approach for determining allowable between reagent lot variation

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), February 2022, De Gruyter

    Dr Marc HM Thelen, Prof Dr em MD PhD EuSpcLM Florent JLA Vanstapel

  2. Validation and verification of examination procedures in medical laboratories: opinion of the EFLM Working Group Accreditation and ISO/CEN standards (WG-A/ISO) on dealing with ISO 15189:2012 demands for method verification and validation

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), February 2020, De Gruyter

    Dr Marc HM Thelen, Professor Christos Kroupis, Prof Dr em MD PhD EuSpcLM Florent JLA Vanstapel

  3. Documenting metrological traceability as intended by ISO 15189:2012: A consensus statement about the practice of the implementation and auditing of this norm element

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), December 2018, De Gruyter

    Dr Marc HM Thelen, Professor Christos Kroupis, Prof Dr em MD PhD EuSpcLM Florent JLA Vanstapel

  4. Harmonization of accreditation to ISO15189

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), January 2018, De Gruyter

    Dr Marc HM Thelen

  5. Technical and clinical validation of the Greiner FC-Mix glycaemia tube

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), January 2017, De Gruyter

    Dr Marc HM Thelen

  6. Expressing analytical performance from multi-sample evaluation in laboratory EQA

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), January 2017, De Gruyter

    Dr Marc HM Thelen

  7. Flexible Scope for ISO15189 accreditation

    Article • Clinical Chemistry and Laboratory Medicine (CCLM), January 2015, De Gruyter

    Professor Christos Kroupis, Dr Marc HM Thelen, Prof Dr em MD PhD EuSpcLM Florent JLA Vanstapel