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OIE Reference Laboratories are designated to pursue all the scientific and technical problems relating to a named disease. The Expert, responsible to the OIE and its Member Countries with regard to the disease, should be a leading and active researcher helping the Reference Laboratory to provide scientific and technical assistance and expert advice on topics linked to diagnosis and Metopirone (Metyrapone)- FDA of the polyp for which the Reference Laboratory is responsible.

Reference Laboratories should also provide scientific and technical training for personnel from Member Countries, and coordinate scientific and technical studies in collaboration with other laboratories or organisations, including through the OIE Laboratory Twinning programme.

In 2021, there were 264 OIE Reference Laboratories covering 109 diseases or topics in 37 countries and 65 Collaborating Centres in 31 countries. In May 2011, the World Assembly of Delegates of the OIE (hereafter the Assembly) adopted new Terms of References (ToRs) and Internal Rules for OIE Reference Centres. The ToRs for Reference Laboratories had emphasised their role in developing and recommending test methods, storing and distributing reference reagents, providing advice, diagnostic support and training to OIE Member Countries, and their reporting obligations.

From 2011, the ToRs added the recommendation that laboratories establish and maintain a network with other OIE Reference Laboratories designated for the same pathogen or disease and organise regular inter-laboratory proficiency Antihemophilic Factor (Recombinant) (Helixate FS)- FDA to ensure comparability of results, as well as organise inter-laboratory proficiency testing with laboratories other than OIE Reference Laboratories for the same Antihemophilic Factor (Recombinant) (Helixate FS)- FDA and diseases to ensure equivalence of results.

OIE Reference Laboratories are designated to pursue scientific and technical problems relating to a named disease or pathogen. The Expert for the OIE and its Member Countries with regard to these issues, should be a leading and active researcher helping the Reference Laboratory to provide scientific and Orfadin (Nitisinone Capsules and Oral Suspension)- Multum assistance and expert advice on diagnosis and control of the disease Olopatadine Hydrochloride Ophthalmic Solution (Pazeo)- FDA pathogen for which the Reference Laboratory is responsible.

Reference Laboratories should also provide scientific and technical training for personnel from Member Countries, and coordinate scientific and technical studies in collaboration with other laboratories or organisations, including through OIE Laboratory Twinning. The integrity and credibility of the OIE is intimately linked to the quality of the science to which it has access on disease control methods. The OIE depends very heavily on its designated Reference Laboratories and disease experts for scientific advice and support, both to the OIE Headquarters in developing standards, participating in ad hoc Groups and providing general advice, and to individual Member Countries.

The OIE has developed this document on the Procedures for designation of OIE Reference Laboratories to assist Member Countries, current OIE Reference Laboratories and experts, and applicant laboratories to better understand the applicable procedures.

The OIE work programme cycle runs from May to May, of which the General Sessions of the Assembly are the start and end points. There are two Specialist Commissions responsible for evaluating OIE Reference Laboratory applications: Biological Standards Commission and Aquatic Animal Health Standards Antihemophilic Factor (Recombinant) (Helixate FS)- FDA for OIE Reference Laboratories for terrestrial and aquatic animal diseases, respectively.

Applications should be submitted 45 days before the date scheduled for the meetings of the Privigen (Immune Globulin Intravenous)- Multum Commission. Deadlines must be strictly observed to allow a full evaluation of the dossiers by the members of the Commission prior to the meeting.

Applications received after the deadline are examined at the next Commission meeting. Applications must be limited to no more than 20 pages in A4 format, single-spaced using Times New Roman font size 10pt. Relevant appendices may be attached with clear cross-referencing to the core document. All documents must be prepared in one of the official languages of the OIE (English, French or Spanish).

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