The national reference laboratory is the leading laboratory in the state which in the specific area official testing has been nominated in accordance with the requirements of EU and national legislation.
Articles 92 and 93 of Regulation (EC) No 2017/625 on official controls replacing Regulation (EC) No 882/2004 from 14.12.2019 require the establishment of European Union reference laboratories and the procedures for their designation. Article 94 sets out the duties and tasks of these laboratories, where cooperation with EU national reference laboratories plays an important role.
Pursuant to Article 147 of Regulation (EC) No 2017/625, the designation of all European Union reference laboratories referred to in Annex VII to Regulation (EC) No 882/2004 shall remain in force until the designation of the European Union reference laboratory in the same field in accordance with Article 93 of this Regulation.
Link to the list of EU Reference Laboratories: https://ec.europa.eu/food/horizontal-topics/european-union-reference-laboratories_en
Article 100 of Regulation (EC) No 2017/625 provides that Member States shall designate one or more national reference laboratories for each EU reference laboratory designated in accordance with Article 93(1). Member States may also designate a national reference laboratory where there is no relevant EU reference laboratory.
The tasks and duties of the national reference laboratory are laid down in Article 101 of the Regulation. National reference laboratories shall, in their area of competence:
Laws:
Regulations of Cabinet of Ministers of the Republic of Latvia and European Union Regulations:
Laboratories of the Institute of Food safety, Animal health and Environment “BIOR” (further on – Institute “BIOR”) have partly been performing the functions of the leading laboratory already since establishment of the Institute. Regulation of Cabinet of Ministers No.834 of 4th December 2007 “Regulation on granting the status of reference laboratory and order of accreditation, functions and duties as well as requirements determined for the equipment and appliances of reference laboratory” listed the area, for which the National Diagnostic Centre of Food and Veterinary Service (now Institute “BIOR”) is nominated as national reference laboratory.
In accordance with the authorisation, the Institute “BIOR” has been nominated as the National Reference Laboratory in the following areas:
Having regard to the fact that laboratory diagnostics is the area in which technological development happens rapidly, the national reference laboratory must ensure immediate fulfilment of all newest requirements and their implementation in official control. In addition to the aforementioned, such a laboratory must be able to develop, optimize and validate the methods of laboratory examinations, as well as to maintain the bank of agent stems and samples, the bank of antigens of agents, a stock of the set of diagnostic regents, specific bank of immunoglobulin and serum, as well as to perform laboratory examinations in the granted area of reference and, in case of disputes, to confirm or refuse the results of laboratories authorized or accredited by the state in the granted area of reference.
The national reference laboratory is the only state laboratory which constantly – 24h per day – maintain the readiness of their technologies and personnel for extraordinary situations and outbreaks of animal infection diseases.
As the official control is performed by considering also the results of examinations performed by the companies dealing with the circulation of animal feed and food in accordance with HACCP programs, it is important to ascertain about the competence of the laboratories of the company which might be achieved by involving these laboratories in the training organized by the national reference laboratory and by participation in inter-laboratory comparative testing organized by it.
In accordance with the legislation the member states must ensure the functions of reference in all appointed areas because in the opposite case the competence of laboratories involved in official control will be disputed at the level of the European Commission, and consequently – the credibility of the official control to be performed in the state. The fulfilment of the reference functions in a full scale will provide a possibility to make a considerable improvement of the ability of Latvia as EU member state, as well as its competence to justify the opinion regarding the perfection of supervision and control mechanisms of various infection disease agents and food pollutants, as well as its regulatory values, which in turn will foster the export capability of the sector.
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