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Published byAgatha Hines Modified over 5 years ago
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IMPLEMENTING DIRECTIVE 2000/60/EC CONCERNING MINIMUM PERFORMANCE CRITERIA FOR CHEMICAL MONITORING METHODS AND THE QUALITY OF ANALYTICAL RESULTS via a Commission Decision working on the WORKING PAPER – Draft version 5
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In a nutshell … Use of validated methods
Laboratories may select any analytical method of their choice for the purpose of monitoring, but must meet minimum performance criteria (LOD, U) Except operational defined parameters : specific standard method obligatory Laboratories to consult CIS Guidance Document Obligatory use of QMS based on ISO/IEC-17025 Requirement to ensure traceability to common standards applying appropriate quality control tools as described in the section 4 of the Annex to this Decision The Member States shall designate competent authorities and bodies responsible for the coordination on their territory of Community-wide quality assurance programmes organized by the Commission or other competent bodies recognised by Member State authorities successfully participation in an appropriate PT organised by the Commission or a competent body approved by Member State authorities Results of participations in PT will be evaluated on the basis of scoring according to ISO-13528, to be linked to the Target Uncertainty values listed in the Annex
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Scoring linked to the target uncertainty in Council Decision
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This approach avoids ‘redundancies’ in the Commission Decision and avoids ‘rapid aging’ and need for frequent updating Reflected in EAF(5) – 04/01/AMPS puts the responsibility for implementation of ISO/IEC with the laboratories and Competent Authorities
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Operationally defined quantity
Your result directly depends on the measurement procedure/protocol Standard methods are essential in this case Typical examples : AOX & EOX leaching tests ecotoxicological methods
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Open discussion points
PTs : What is successful participation? Who is responsible to assesses this ? ‘designate C.A. and bodies responsible for the coordination QA programmes’ : what do we mean ? Provision of which QA tools (access to PT, RM, training) ? Who assesses QMS ? By the way : in the GW Guidance document accreditation is set
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Accreditation … ? Either not required at all
Or a way out : a laboratory to be accredited for 1/10 of monitoring analyses it provides 1/2 of monitoring analyses accredited …. Advantage : a real commitment to quality, imbedded in management system
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