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  1. #2064979

    le haghaidh ionfhabhtú le Brucella abortus, Brucella melitensis agus Brucella suis, tástáil shéireolaíoch dá dtagraítear i bpointe 1 de Chuid 1 d’Iarscríbhinn I a ghabhann le Rialachán Tarmligthe (AE) 2020/688;

    for infection with Brucella abortus, Brucella melitensis and Brucella suis, a serological test referred to in point 1 of Part 1 of Annex I to Delegated Regulation (EU) 2020/688;

    Commission Delegated Regulation (EU) 2021/880 of 5 March 2021 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards the traceability, animal health and certification requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  2. #2706093

    cuireadh faoi thástáil shéireolaíoch i leith eipididimitis caorach (Brucella ovis) iad, ar tástáil í lenar ghabh torthaí diúltacha, i rith na tréimhse 30 lá roimh an dáta seolta chuig an Aontas.”,

    they were subjected to a serological test for ovine epididymitis (Brucella ovis), with negative results, during the period of 30 days prior to the date of dispatch to the Union.’;

    Commission Delegated Regulation (EU) 2023/119 of 9 November 2022 amending Delegated Regulation (EU) 2020/692 supplementing Regulation (EU) 2016/429 of the European Parliament and of the Council as regards rules for entry into the Union, and the movement and handling after entry of consignments of certain animals, germinal products and products of animal origin (Text with EEA relevance)

  3. #2718906

    rinneadh an tástáil shéireolaíoch ar shamplaí arna mbailiú le linn na tréimhse 60 lá ar a laghad roimh dháta imeachta na coinsíneachta;]]

    the serological test has been carried out on samples collected during the period of at least 60 days prior to the date of departure of the consignment;]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  4. #2861520

    an líon bunaíochtaí ina gcoimeádtar bó-ainmhithe a ndearnadh tástáil orthu le tástáil séireolaíochta le haghaidh ionfhabhtú le Brucella abortus, B. melitensis agus B. suis gach bliain le 3 bliana anuas;

    number of establishments keeping bovine animals tested with a serological test for infection with Brucella abortus, B. melitensis and B. suis each year for the last three years;

    Commission Implementing Regulation (EU) 2023/1451 of 13 July 2023 amending Implementing Regulation (EU) 2020/2002 as regards disease notification and the information to be submitted by the Member States for the approval and reporting of compulsory and optional eradication programmes and in applications for disease-free status (Text with EEA relevance)

  5. #308652

    (17) Le hAirteagal 23 de Rialachán (CE) Uimh. 998/2003, foráiltear go ndéanfaidh an Coimisiún, tar éis dó tuairim a fháil ón Údarás Eorpach um Shábháilteacht Bia (EFSA) maidir leis an ngá leis an tástáil shéireolaíoch a choimeád ar bun, agus ar bhonn na taithí a bheidh faighte agus ar bhonn meastóireachta riosca, tuarascáil a chur faoi bhráid Pharlaimint na hEorpa agus na Comhairle, mar aon le tograí iomchuí chun an réimeas a chinneadh a bheidh le cur i bhfeidhm le héifeacht ón 1 Iúil 2010 le haghaidh Airteagal 6, Airteagal 8 agus Airteagal 16 den Rialachán sin.

    (17) Article 23 of Regulation (EC) No 998/2003 provides that the Commission, after receipt of the opinion of the European Food Safety Authority (EFSA) on the need to maintain the serological test, and based on experience gained and on a risk evaluation, is to submit to the European Parliament and to the Council a report, together with appropriate proposals for determining the regime to be applied with effect from 1 July 2010 for Articles 6, 8 and 16 of that Regulation.

    Regulation (EU) No 438/2010 of the European Parliament and of the Council of 19 May 2010 amending Regulation (EC) No 998/2003 on the animal health requirements applicable to the non-commercial movement of pet animals

  6. #308654

    (19) An 11 Nollaig 2006, ghlac EFSA tuairim dar teideal "Measúnú ar an riosca go dtabharfar confadh isteach sa Ríocht Aontaithe, in Éirinn, sa tSualainn agus i Málta, de dhroim éirí as an tástáil shéireolaíoch lena dtomhaistear antasubstaintí cosantacha i gcoinne confaidh" [6].

    (19) On 11 December 2006, EFSA adopted an opinion entitled "Assessment of the risk of rabies introduction into the UK, Ireland, Sweden, Malta, as a consequence of abandoning the serological test measuring protective antibodies to rabies" [6].

    Regulation (EU) No 438/2010 of the European Parliament and of the Council of 19 May 2010 amending Regulation (EC) No 998/2003 on the animal health requirements applicable to the non-commercial movement of pet animals

  7. #338269

    Chuige sin agus de bhun Airteagal 23 de Rialachán (CE) Uimh. 998/2003, ceanglaíodh ar an gCoimisiún tuarascáil a chur faoi bhráid Pharlaimint na hEorpa agus faoi bhráid na Comhairle, roimh an 1 Feabhra 2007, maidir leis an ngá atá leis an tástáil shéireolaíoch a choinneáil, mar aon le tograí iomchuí chun an córas a chinneadh a chuirfear i bhfeidhm tar éis na gcóras idirthréimhseach dá bhforáiltear in Airteagal 6, in Airteagal 8 agus in Airteagal 16 den Rialachán sin.

    To that end and pursuant to Article 23 of Regulation (EC) No 998/2003, the Commission was required to submit to the European Parliament and to the Council, before 1 February 2007, a report on the need to maintain the serological test, together with appropriate proposals for determining the regime to be applied after the transitional regimes provided for in Articles 6, 8 and 16 of that Regulation.

    Regulation (EC) No 454/2008 of the European Parliament and of the Council of 21 May 2008 amending Regulation (EC) No 998/2003 on the animal health requirements applicable to the non-commercial movements of pet animals, as regards the extension of the transitional period

  8. #2064974

    maidir le leoicéime bhuaibheach eansótach, tástáil shéireolaíoch dá dtagraítear i bpointe (a) de Chuid 4 d’Iarscríbhinn I a ghabhann le Rialachán Tarmligthe (AE) 2020/688, ach amháin má tá feidhm ag an maolú dá bhforáiltear in Airteagal 20(2)(a) den Rialachán seo;”;

    for enzootic bovine leukosis, a serological test referred to in point (a) of Part 4 of Annex I to Delegated Regulation (EU) 2020/688, unless the derogation provided for in Article 20(2)(a) of this Regulation applies;’;

    Commission Delegated Regulation (EU) 2021/880 of 5 March 2021 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards the traceability, animal health and certification requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  9. #2064977

    i gcás ainmhithe den chineál caorach, ní mór dóibh teacht ó bhunaíocht ina ndearnadh tástáil shéireolaíoch orthu le haghaidh eipididimíteas caorach (Brucella ovis), nó aon tástáil eile le haghaidh eipididimíteas caorach (Brucella ovis); a bhfuil íogaireacht agus sainiúlacht choibhéiseach dhoiciméadaithe aici, agus an tástáil sin a bheith déanta orthu agus ar aon ainmhí fireann den chineál gabhair a choimeádtar in éineacht leo, tástáil a raibh torthaí diúltacha uirthi, le linn thréimhse 60 lá sula gcuirtear iad chun fanacht sa chóiríocht choraintín dá dtagraítear i bpointe (a);

    in the case of ovine animals, they must come from an establishment where, during the period of 60 days prior to their stay in the quarantine accommodation referred to in point (a), they, and any male caprine animal kept with them together, have been subjected with negative results to a serological test for ovine epididymitis (Brucella ovis), or any other test for ovine epididymitis (Brucella ovis) of an equivalent documented sensitivity and specificity;

    Commission Delegated Regulation (EU) 2021/880 of 5 March 2021 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards the traceability, animal health and certification requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  10. #2064980

    i gcás ainmhithe den chineál caorach agus aon ainmhí fireann den chineál gabhair a choimeádtar in éineacht leo, tástáil shéireolaíoch le haghaidh eipididimíteas caorach (Brucella ovis), nó aon tástáil eile le haghaidh eipididimíteas caorach (Brucella ovis) a bhfuil íogaireacht agus sainiúlacht choibhéiseach dhoiciméadaithe aici;

    in the case of ovine animals, and any male caprine animals kept with them together, a serological test for ovine epididymitis (Brucella ovis), or any other test for ovine epididymitis (Brucella ovis) of an equivalent documented sensitivity and specificity;

    Commission Delegated Regulation (EU) 2021/880 of 5 March 2021 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards the traceability, animal health and certification requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  11. #2064982

    i gcás ainmhithe den chineál caorach, agus aon ainmhí fireann den chineál gabhair a choimeádtar in éineacht leo, tástáil shéireolaíoch le haghaidh eipididimíteas caorach (Brucella ovis), nó aon tástáil eile le haghaidh eipididimíteas den chineál caorach (Brucella ovis) a bhfuil íogaireacht agus sainiúlacht choibhéiseach dhoiciméadaithe acu.”;

    in the case of ovine animals, and any male caprine animals kept with them together, a serological test for ovine epididymitis (Brucella ovis), or any other test for ovine epididymitis (Brucella ovis) of an equivalent documented sensitivity and specificity.’;

    Commission Delegated Regulation (EU) 2021/880 of 5 March 2021 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards the traceability, animal health and certification requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  12. #2074238

    Bunaithe ar threoir arna fáil de bhun Airteagal 3(11), tugtar de chumhacht don Choimisiún gníomhartha tarmligthe a ghlacadh i gcomhréir le hAirteagal 12 chun mír 1 den Airteagal seo agus pointe (c) d' Airteagal 3(1) a leasú chun foráil a dhéanamh maidir leis an deimhniú téarnaimh a eisiúint ar bhonn mearthástáil dhearfach antaiginí, tástáil antasubstainte, lena n-áiritear tástáil shéireolaíoch le haghaidh antasubstaintí i gcoinne SARS-CoV-2, nó aon mhodh eile atá bailíochtaithe go heolaíoch.

    On the basis of guidance received pursuant to Article 3(11), the Commission is empowered to adopt delegated acts in accordance with Article 12 to amend paragraph 1 of this Article and point (c) of Article 3(1) to allow for the issuance of the certificate of recovery on the basis of a positive rapid antigen test, antibody test, including a serological test for antibodies against SARS-CoV-2, or any other scientifically validated method.

    Regulation (EU) 2021/953 of the European Parliament and of the Council of 14 June 2021 on a framework for the issuance, verification and acceptance of interoperable COVID-19 vaccination, test and recovery certificates (EU Digital COVID Certificate) to facilitate free movement during the COVID-19 pandemic (Text with EEA relevance)

  13. #2087967

    rinneadh tástáil shéireolaíoch orthu chun antasubstaintí sonracha in aghaidh víreas ghalar an chraicinn chnapánaigh a bhrath lá an bhailithe agus ar a laghad 28 lá tar éis na tréimhse bailithe a mhéid a bhaineann le seamhan nó lá an bhailithe a mhéid a bhaineann le suthanna agus ubháin, tástáil a raibh torthaí diúltacha uirthi;

    subjected to a serological test to detect specific antibodies against the LSDV on the day of the collection and at least 28 days after the period of collection as regards semen or on the day of collection as regards embryos and ova, with negative results;

    Commission Implementing Regulation (EU) 2021/1070 of 28 June 2021 laying down special control measures for a limited period of time related to infection with lumpy skin disease virus (Text with EEA relevance)

  14. #2305805

    ar feadh 28 lá ar a laghad roimh dháta seolta na n-ainmhithe chuig an Aontas agus gur cuireadh na hainmhithe faoi thástáil shéireolaíoch i gcomhréir le hAirteagal 9, pointe (b), de Rialachán Tarmligthe (AE) 2020/692, agus a raibh torthaí diúltacha ar an tástáil sin, arna déanamh ar shamplaí a bailíodh 28 lá ar a laghad tar éis dháta iontrála an ainmhí sa chrios lena mbaineann saoirse shéasúrach.] (1)(6)

    for at least 28 days prior to the date of dispatch of the animals to the Union and the animals have been subjected to a serological test in accordance with Article 9, point (b), of Delegated Regulation (EU) 2020/692, with negative results, carried out on samples collected at least 28 days following the date of entry of the animal into the seasonally free zone.] (1)(6)

    Commission Implementing Regulation (EU) 2022/250 of 21 February 2022 amending Implementing Regulation (EU) 2021/403 as regards the addition of a new model animal health/official certificate for the entry into Northern Ireland of ovine and caprine animals from Great Britain and amending Implementing Regulation (EU) 2021/404 as regards the list of third countries authorised for the entry into the Union of ovine and caprine animals (Text with EEA relevance)

  15. #2305810

    nach bhfuil saor ó ionfhabhtú leis an víreas gormtheanga (séiritíopaí 1-24) agus cuireadh na hainmhithe faoi thástáil shéireolaíoch, lenar bhain toradh deimhneach, is féidir antasubstaintí sonracha a bhrath in aghaidh na séiritíopaí uile (1 go 24) den víreas gormtheanga a tuairiscíodh le 2 bhliain anuas sa chrios sin, agus:

    is not free from infection with bluetongue virus (serotypes 1-24) and the animals have been subjected with positive results to a serological test able to detect specific antibodies against all serotypes (1 to 24) of bluetongue virus reported during the past 2 years in that zone, and:

    Commission Implementing Regulation (EU) 2022/250 of 21 February 2022 amending Implementing Regulation (EU) 2021/403 as regards the addition of a new model animal health/official certificate for the entry into Northern Ireland of ovine and caprine animals from Great Britain and amending Implementing Regulation (EU) 2021/404 as regards the list of third countries authorised for the entry into the Union of ovine and caprine animals (Text with EEA relevance)

  16. #2305811

    go ndearnadh an tástáil shéireolaíoch ar shamplaí a bailíodh ar a laghad 60 lá roimh dháta seolta na n-ainmhithe chuig an Aontas.]](1)

    the serological test has been carried out on samples collected at least 60 days prior to the date of dispatch of the animals to the Union.]](1)

    Commission Implementing Regulation (EU) 2022/250 of 21 February 2022 amending Implementing Regulation (EU) 2021/403 as regards the addition of a new model animal health/official certificate for the entry into Northern Ireland of ovine and caprine animals from Great Britain and amending Implementing Regulation (EU) 2021/404 as regards the list of third countries authorised for the entry into the Union of ovine and caprine animals (Text with EEA relevance)

  17. #2305812

    go ndearnadh an tástáil shéireolaíoch ar shamplaí a bailíodh ar a laghad 30 lá roimh dháta seolta na n-ainmhithe chuig an Aontas agus cuireadh na hainmhithe faoi thástáil PCR, lenar bhain torthaí diúltacha, arna déanamh ar shamplaí a bailíodh tráth nach luaithe ná 14 lá roimh dháta seolta na n-ainmhithe chuig an Aontas.]](1)

    the serological test has been carried out on samples collected at least 30 days prior to the date of dispatch of the animals to the Union and the animals were subjected to a PCR test, with negative results, carried out on samples collected not earlier than 14 days prior to the date of dispatch of the animals to the Union.]](1)

    Commission Implementing Regulation (EU) 2022/250 of 21 February 2022 amending Implementing Regulation (EU) 2021/403 as regards the addition of a new model animal health/official certificate for the entry into Northern Ireland of ovine and caprine animals from Great Britain and amending Implementing Regulation (EU) 2021/404 as regards the list of third countries authorised for the entry into the Union of ovine and caprine animals (Text with EEA relevance)

  18. #2305845

    go gcuimsítear fireannaigh neamhchoillte d’ainmhithe den chineál caorach, ar ainmhithe iad a d’fhan ar feadh tréimhse leanúnach 60 lá ar a laghad roimh a seoladh chuig an Aontas i mbunaíocht nár tuairiscíodh ionfhabhtú le Brucella ovis (eipididimíteas caorach) inti le linn na tréimhse 12 mhí roimh dháta a seolta chuig an Aontas agus ar cuireadh faoi thástáil shéireolaíoch iad chun Brucella ovis a bhrath, tástáil a raibh torthaí diúltacha uirthi, le linn na 30 lá roimh dháta a seolta chuig an Aontas.] (1)

    include uncastrated males of ovine animals, which have remained for a continuous period of at least 60 days prior to their dispatch to the Union in an establishment where infection with Brucella ovis (contagious epididymitis) has not been reported during the period of 12 months prior to the date of their dispatch to the Union and have been subjected to a serological test for the detection of Brucella ovis, with negative results, during the 30 days prior to the date of their dispatch to the Union.] (1)

    Commission Implementing Regulation (EU) 2022/250 of 21 February 2022 amending Implementing Regulation (EU) 2021/403 as regards the addition of a new model animal health/official certificate for the entry into Northern Ireland of ovine and caprine animals from Great Britain and amending Implementing Regulation (EU) 2021/404 as regards the list of third countries authorised for the entry into the Union of ovine and caprine animals (Text with EEA relevance)

  19. #2469750

    Ar bhonn na treorach a fuarthas de bhun Airteagal 3(11), tugtar de chumhacht don Choimisiún gníomhartha tarmligthe a ghlacadh i gcomhréir le hAirteagal 12 chun mír 1 den Airteagal seo agus Airteagal 3(1), pointe (c), a leasú chun foráil a dhéanamh maidir leis an deimhniú téarnaimh a eisiúint ar bhonn tástáil dhearfach antaiginí, tástáil antasubstainte, lena n-áiritear tástáil shéireolaíoch le haghaidh antasubstaintí i gcoinne SARS-CoV-2, nó aon mhodh eile atá bailíochtaithe go heolaíoch.

    On the basis of guidance received pursuant to Article 3(11), the Commission is empowered to adopt delegated acts in accordance with Article 12 to amend paragraph 1 of this Article and point (c) of Article 3(1) to allow for the issuance of the certificate of recovery on the basis of a positive antigen test, antibody test, including a serological test for antibodies against SARS-CoV-2, or any other scientifically validated method.

    Regulation (EU) 2022/1034 of the European Parliament and of the Council of 29 June 2022 amending Regulation (EU) 2021/953 on a framework for the issuance, verification and acceptance of interoperable COVID-19 vaccination, test and recovery certificates (EU Digital COVID Certificate) to facilitate free movement during the COVID-19 pandemic (Text with EEA relevance)

  20. #2706102

    coimeádadh na hainmhithe ar leithlis i mbunaíochtaí atá cosanta ar veicteoirí ar feadh tréimhse 30 lá ar a laghad roimh an dáta seolta chuig an Aontas agus cuireadh tástáil shéireolaíoch orthu i leith antashubstaintí in aghaidh víreas thinneas Afracach na gcapall a bhrath, ar tástáil í a rinne an tsaotharlann chéanna, an lá céanna, ar shampla fola a tógadh i rith na tréimhse leithlise i mbunaíochtaí atá cosanta ar veicteoirí ar dhá ócáid a raibh eatramh idir 21 lá agus 30 lá ann eatarthu,

    the animals were kept in isolation in vector-protected establishments for a period of at least 30 days prior to the date of dispatch to the Union and underwent a serological test for the detection of antibodies against the African horse sickness virus, carried out by the same laboratory, on the same day, on blood samples taken during the isolation period in vector-protected establishments on two occasions with an interval of between 21 and 30 days.

    Commission Delegated Regulation (EU) 2023/119 of 9 November 2022 amending Delegated Regulation (EU) 2020/692 supplementing Regulation (EU) 2016/429 of the European Parliament and of the Council as regards rules for entry into the Union, and the movement and handling after entry of consignments of certain animals, germinal products and products of animal origin (Text with EEA relevance)

  21. #2718887

    ar feadh na tréimhse 28 lá ar a laghad roimh dháta imeachta na coinsíneachta agus cuireadh faoi thástáil shéireolaíoch iad, agus torthaí diúltacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse 28 lá ar a laghad tar éis dháta theacht isteach an ainmhí sa Bhallstát nó sa chrios den Bhallstát atá saor go séasúrach ó ionfhabhtú leis an víreas gormtheanga (séiritíopaí 1-24);]]

    for the period of at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected during the period of at least 28 days following the date of entry of the animal into the Member State or zone thereof seasonally free from infection with bluetongue virus (serotypes 1-24);]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  22. #2718894

    ar feadh na tréimhse 28 lá ar a laghad roimh dháta imeachta na coinsíneachta agus cuireadh na hainmhithe faoi thástáil shéireolaíoch, agus torthaí diúltacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse 28 lá ar a laghad tar éis dháta tosaigh na tréimhse cosanta ar ionsaithe ó veicteoirí;]]

    for the period of at least 28 days prior to the date of departure of the consignment and have been subjected to a serological test, with negative results, carried out on samples collected during the period of at least 28 days following the date of the commencement of the period of protection against attacks by vectors;]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  23. #2718904

    cuireadh faoi thástáil shéireolaíoch iad, agus torthaí dearfacha uirthi, lenar féidir antasubstaintí sonracha in aghaidh gach steiréitíopa 1-24 den ionfhabhtú leis an víreas gormtheanga a bhrath ar tuairiscíodh gurbh ann dó sa Bhallstát sin nó i gcrios de le linn na tréimhse 2 bhliain roimh dháta imeachta na coinsíneachta, agus:

    have been subjected with positive results to a serological test able to detect specific antibodies against all serotypes 1-24 of infection with bluetongue virus reported in that Member State or zone thereof during the period of 2 years prior to the date of departure of the consignment, and:

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  24. #2718908

    rinneadh an tástáil shéireolaíoch ar shamplaí arna mbailiú le linn na tréimhse 30 lá ar a laghad roimh dháta imeachta na coinsíneachta agus cuireadh an t-ainmhí faoi thástáil PCR, agus torthaí diúltacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse tráth nach luaithe ná 14 lá roimh dháta imeachta na coinsíneachta;]]]

    the serological test has been carried out on samples collected during the period of at least 30 days prior to the date of departure of the consignment and the animal has been subjected to a PCR test, with negative results, carried out on samples collected during the period of not earlier than 14 days prior to the date of departure of the consignment;]]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  25. #2718918

    cuireadh na hainmhithe faoi thástáil shéireolaíoch, agus torthaí dearfacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse 60 lá ar a laghad roimh dháta imeachta na coinsíneachta;]]]

    the animals have been subjected with positive results to a serological test carried out on samples collected during the period of at least 60 days prior to the date of departure of the consignment;]]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  26. #2718920

    cuireadh na hainmhithe faoi thástáil shéireolaíoch, agus torthaí dearfacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse 30 lá ar a laghad roimh dháta imeachta na coinsíneachta agus faoi thástáil PCR, agus torthaí diúltacha uirthi, arna déanamh ar shamplaí arna mbailiú le linn na tréimhse tráth nach luaithe ná 14 lá roimh dháta imeachta na coinsíneachta.]]]]

    the animals have been subjected with positive results to a serological test carried out on samples collected during the period of at least 30 days prior to the date of departure of the consignment and to a PCR test, with negative results, carried out on samples collected during the period of not earlier than 14 days prior to the date of departure of the consignment.]]]]

    Commission Implementing Regulation (EU) 2023/308 of 8 February 2023 amending Annex I to Implementing Regulation (EU) 2021/403 as regards model animal health certificates for movements between Member States of consignments of cervid animals (Text with EEA relevance)

  27. #2720420

    aon bhunaíocht, tar éis toradh diúltach a fháil i dtástáil shéireolaíoch chun antashubstaint a bhrath in aghaidh víreas GCB a rinneadh ar shampla fola a tógadh sular seoladh ón mbunaíocht tionscnaimh é.

    any establishment, after having obtained a negative result in a serological test for the detection of antibody against the FMD virus carried out on a sample of blood taken prior to dispatch from the establishment of origin;

    Commission Delegated Regulation (EU) 2023/361 of 28 November 2022 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards rules for the use of certain veterinary medicinal products for the purpose of prevention and control of certain listed diseases (Text with EEA relevance)

  28. #2720503

    rinneadh tástáil shéireolaíoch orthu, tástáil a raibh torthaí diúltacha uirthi chun antasubstaintí sonracha in aghaidh víreas ghalar an chraicinn chnapánaigh a bhrath lá an bhailithe agus ar a laghad 28 lá tar éis na tréimhse bailithe a mhéid a bhaineann le seamhan nó ar lá an bhailithe a mhéid a bhaineann le suthanna agus úicítí;

    subjected, with negative results, to a serological test to detect specific antibodies against LSD virus on the day of the collection and at least 28 days after the period of collection as regards semen or on the day of collection as regards embryos and oocytes;

    Commission Delegated Regulation (EU) 2023/361 of 28 November 2022 supplementing Regulation (EU) 2016/429 of the European Parliament and the Council as regards rules for the use of certain veterinary medicinal products for the purpose of prevention and control of certain listed diseases (Text with EEA relevance)

  29. #2734264

    maidir le hionfhabhtú le víreas siondróim atáirgthe agus riospráide mhucúil, tástáil shéireolaíoch (IPMA, IFA, nó ELISA) nó tástáil ar ghéanóm víris (imoibriú slabhrúil polaiméaráise cúl-trascrioptáise (ISP- CT), ISP-CT neadaithe, ISP-CT fíor-ama).

    as regards infection with porcine reproductive and respiratory syndrome virus, a serological test (IPMA, IFA, or ELISA) or a test for virus genome (reverse-transcription polymerase chain reaction (RT-PCR), nested set RT-PCR, real-time RT-PCR).

    Commission Delegated Regulation (EU) 2023/647 of 13 January 2023 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and of the Council as regards the approval of germinal product establishments and the traceability and animal health requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  30. #2734280

    cuireadh tástáil shéireolaíoch orthu chun antashubstaintí i leith ionfhabhtú le víreas an ghalair fuilreatha eipeasótaigh a bhrath, a raibh torthaí diúltacha uirthi, gach 60 lá ar a laghad le linn na tréimhse bailiúcháin agus idir 28 agus 60 lá ó dháta bailithe deiridh an tseamhain;

    they have been subjected to a serological test to detect antibodies to infection with epizootic haemorrhagic disease virus, with negative results, at least every 60 days throughout the collection period and between 28 and 60 days from the date of the final collection of the semen;

    Commission Delegated Regulation (EU) 2023/647 of 13 January 2023 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and of the Council as regards the approval of germinal product establishments and the traceability and animal health requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  31. #2734288

    cuireadh tástáil shéireolaíoch orthu chun antashubstaintí i leith ionfhabhtú le víreas an ghalair fuilreatha eipeasótaigh a bhrath, a raibh torthaí diúltacha uirthi, ar shampla fola a tógadh idir 28 agus 60 lá ó dháta bailithe na n-úicítí nó na suthanna;

    they have been subjected to a serological test to detect antibodies to infection with epizootic haemorrhagic disease virus, with negative results, on a blood sample taken between 28 and 60 days from the date of collection of the oocytes or embryos;

    Commission Delegated Regulation (EU) 2023/647 of 13 January 2023 amending Delegated Regulation (EU) 2020/686 supplementing Regulation (EU) 2016/429 of the European Parliament and of the Council as regards the approval of germinal product establishments and the traceability and animal health requirements for movements within the Union of germinal products of certain kept terrestrial animals (Text with EEA relevance)

  32. #3033952

    ar feadh 28 lá ar a laghad roimh dháta na gluaiseachta agus rinneadh tástáil shéireolaíoch orthu, tástáil a raibh torthaí diúltacha uirthi, arna déanamh ar shamplaí a bailíodh 28 lá ar a laghad i ndiaidh dháta iontrála an ainmhí isteach sa limistéar atá saor go séasúrach ó ghalar; nó

    for at least 28 days prior to the date of movement and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the entry date of the animal into the seasonally disease-free area; or

    Commission Delegated Regulation (EU) 2023/2515 of 8 September 2023 amending Delegated Regulation (EU) 2020/688 as regards certain animal health requirements for movements within the Union of terrestrial animals

  33. #3033955

    ar feadh 28 lá ar a laghad roimh dháta na gluaiseachta agus rinneadh tástáil shéireolaíoch orthu, tástáil a raibh torthaí diúltacha uirthi, arna déanamh ar shamplaí a bailíodh 28 lá ar a laghad i ndiaidh dháta tosaigh na tréimhse cosanta ar ionsaithe ó veicteoirí; nó

    for at least 28 days prior to the date of movement and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the date of the commencement of the period of protection against attacks by vectors; or

    Commission Delegated Regulation (EU) 2023/2515 of 8 September 2023 amending Delegated Regulation (EU) 2020/688 as regards certain animal health requirements for movements within the Union of terrestrial animals

  34. #3033964

    ar feadh 28 lá ar a laghad roimh dháta na gluaiseachta agus rinneadh tástáil shéireolaíoch orthu, tástáil a raibh torthaí diúltacha uirthi, arna déanamh ar shamplaí a bailíodh 28 lá ar a laghad i ndiaidh dháta iontrála an ainmhí isteach sa limistéar atá saor go séasúrach ó ghalar; nó

    for at least 28 days prior to the date of movement and have been subjected to a serological test, with negative results, carried out on samples collected at least 28 days following the entry date of the animal into the seasonally disease -free area; or

    Commission Delegated Regulation (EU) 2023/2515 of 8 September 2023 amending Delegated Regulation (EU) 2020/688 as regards certain animal health requirements for movements within the Union of terrestrial animals