- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (31/12/2020)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Commission Delegated Regulation (EU) 2020/687 of 17 December 2019 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council, as regards rules for the prevention and control of certain listed diseases (Text with EEA relevance)
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Point in time view as at 31/12/2020.
There are currently no known outstanding effects for the Commission Delegated Regulation (EU) 2020/687, ANNEX I.
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animals showing clinical signs of category A diseases;
animals likely to have recently died from the suspected/confirmed disease;
animals with epidemiological link to a suspected or confirmed case; and
animals that obtained positive or non-conclusive results in previous laboratory examinations.
the purpose of the sampling;
the listed species kept in the establishment;
the number of animals of listed species kept in the establishment;
the category of the kept animals;
the available production, health and traceability records of the kept animals relevant for the investigation;
the type of establishment and the husbandry practices;
the level of exposure risk:
likelihood of exposure to the disease agent or to the vector;
absence of immunisation of the animals due to vaccination or maternal immunity; and
history of residence in the establishment;
other relevant epidemiological factors.
the expected prevalence in the establishment;
the level of confidence desired of the survey results, which in any case must not be lower than 95 %; and
international standards and available scientific evidence.
The techniques, reference materials, their standardisation and the interpretation of the results of tests carried out using the relevant diagnostic methods for category A diseases must comply with Article 6 and Part III of Annex VI to Delegated Regulation (EU) 2020/689.
The diagnostic methodology must aim to maximise the sensitivity of the surveillance. In certain circumstances this surveillance may include the use of laboratory examinations in order to assess previous exposure to disease.
the establishment of origin of the sampled animals;
information on the species, age and category of the sampled animals;
the clinical history of the animals, if available and relevant;
the clinical signs and post-mortem findings; and
any other relevant information.
stored in watertight and unbreakable containers and packages and in accordance with applicable international standards;
kept at the most appropriate temperature and other conditions during transport taking into account the factors that may affect the sample quality.
‘Animal pathological material; perishable; fragile; do not open outside the laboratory of destination.’
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