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REGULATION (EU) 2025/13 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
of 19 December 2024
on the collection and transfer of advance passenger information for the prevention, detection, investigation and prosecution of terrorist offences and serious crime, and amending Regulation (EU) 2019/818
Having regard to the Treaty on the Functioning of the European Union,
Having regard to Council Decision 2009/470/EC of 25 May 2009 on expenditure in the veterinary field (1), and in particular Article 27(5) thereof,
Whereas:
(1) Decision 2009/470/EC lays down the procedures governing the Union financial contribution for programmes for the eradication, control and monitoring of animal diseases and zoonoses.
(2) In addition, Article 27(1) of Decision 2009/470/EC provides that a Union financial measure is to be introduced to reimburse the expenditure incurred by the Member States for the financing of national programmes for the eradication, control and monitoring of the animal diseases and zoonoses listed in Annex 1 to that Decision.
(3) Commission Decision 2008/341/EC of 25 April 2008 laying down Community criteria for national programmes for the eradication, control and monitoring of certain animal diseases and zoonoses (2) provides that in order to be approved under the Union financial measures, programmes submitted by the Member States must meet at least the criteria set out in the Annex to that Decision.
(4) Regulation (EC) No 999/2001 of the European Parliament and of the Council of 22 May 2001 laying down rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies (3) provides for annual monitoring programmes by Member States for transmissible spongiform encephalopathies (TSEs) in bovine, ovine and caprine animals.
(5) Council Directive 2005/94/EC of 20 December 2005 on Community measures for the control of avian influenza (4) also provides for surveillance programmes by Member States to be carried out in respect of poultry and wild birds in order to contribute, inter alia, on the basis of regularly updated risk-assessments, to the knowledge on the threats posed by the wild birds in relation to any influenza virus of avian origin in birds. Those annual programmes, and their financing, for monitoring should also be approved.
(6) Certain Member States have submitted to the Commission annual programmes for the eradication, control and monitoring of animal diseases, programmes of checks aimed at the prevention of zoonoses, and annual monitoring programmes for the eradication and monitoring of certain TSEs for which they wish to receive a financial contribution from the Union.
(7) For the years 2008, 2009, 2010 and 2011 certain multiannual programmes submitted by Member States for the eradication, control and monitoring of the animal diseases were approved under Commission Decisions 2007/782/EC (5), 2008/897/EC (6), 2009/883/EC (7) and 2010/712/EU (8).
(8) The commitment of the expenditure for those multiannual programmes was adopted in accordance with Article 76(3) of Council Regulation (EC, Euratom) No 1605/2002 of 25 June 2002 on the Financial Regulation applicable to the general budget of the European Communities (9). The first budget commitment for those programmes was made after their approval. Each subsequent annual commitment should be made by the Commission in function of the execution of the programme for the previous year, on the basis of a decision to grant a contribution referred to in Article 27(5) of Decision 2009/470/EC.
(9) Certain Member States which have been successfully implementing rabies eradication programmes that have been co-financed for several years, share land borders with third countries where that disease is present. In order to finally eradicate rabies, certain vaccination activities need to be carried out in the territory of those third countries adjacent to the Union.
(10) In order to support the implementation of rabies vaccination activities to be carried out in the territory of those third countries adjacent to the Union, the payment of an advance of up to 60 % of the maximum amount set for such activities under the Member State programmes, should be made possible.
(11) The Commission has assessed the annual programmes submitted by the Member States, as well as the fifth, fourth, third and second years respectively of the multiannual programmes approved for 2008, 2009, 2010 and 2011, from both the veterinary and financial point of view. Those programmes comply with the relevant Union veterinary legislation and in particular with the criteria set out in Decision 2008/341/EC.
(12) In the light of the importance of the annual and multiannual programmes for the achievement of Union objectives in the field of animal and public health, as well as the obligatory application in all Member States in the case of the Transmissible spongiform encephalopathies (TSE) and avian influenza programmes, it is appropriate to fix the appropriate rate of the Union financial contribution to reimburse the costs to be incurred by the Member States concerned for the measures referred to in this Decision up to a maximum amount for each programme.
(13) In accordance with Article 75 of the Financial Regulation and Article 90(1) of the Implementing Rules, the commitment of expenditure from the Union budget shall be preceded by a financing Decision setting out the essential elements of the action involving expenditure and adopted by the institution or the authorities to which powers have been delegated by the institution.
(14) Verification of individual justifications of eligible costs creates extensive administrative burdens while not notably increasing the efficient use of Union funds or transparency. It is thus more appropriate to fix the Union financial contribution, for each programme, where appropriate, at a level that ensures that costs entailed by the type of measure, if implemented are adequately covered. Union financial contribution supporting in particular defined activities such as sampling, testing and vaccination should accordingly be specified as lump sum intended to compensate for all costs normally incurred to perform the activity or to produce the respective test result.
(15) Under Council Regulation (EC) No 1290/2005 of 21 June 2005 on the financing of the common agricultural policy (10), programmes for the eradication and control of animal diseases are to be financed under the European Agricultural Guarantee Fund. For financial control purposes, Articles 9, 36 and 37 of that Regulation are to apply.
(16) The financial contribution from the Union should be granted subject to the condition that the actions planned are efficiently carried out and that the competent authorities supply all the necessary information within the time limits laid down in this Decision.
(17) For reasons of administrative efficiency all expenditure submitted for a financial contribution by the Union should be expressed in euro. In accordance with Regulation (EC) No 1290/2005, the conversion rate for expenditure in a currency other than the euro should be the most recent exchange rate set by the European Central Bank prior to the first day of the month in which the application is submitted by the Member State concerned.
(18) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic animal sampled;
(ii) EUR 0,2 per rose bengal test;
(iii) EUR 0,2 per SAT test;
(iv) EUR 0,4 per complement fixation test;
(v) EUR 0,5 per ELISA test;
(vi) EUR 10 per bacteriological test;
(vii) EUR 1 per domestic animal vaccinated;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State referred to in paragraph 1 for the cost of the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes and shall on average not exceed EUR 375 per animal slaughtered; and
(c) shall not exceed the following:
(i) EUR 4 800 000 for Spain;
(ii) EUR 2 300 000 for Italy;
(iii) EUR 1 550 000 for Portugal;
(iv) EUR 2 000 000 for the United Kingdom.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic animal sampled;
(ii) EUR 1,5 per tuberculin test;
(iii) EUR 5 per gamma-interferon test;
(iv) EUR 10 per bacteriological test;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State referred to in paragraph 1 for the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes shall on average not exceed EUR 375 per animal slaughtered; and
(c) shall not exceed the following:
(i) EUR 14 000 000 for Ireland;
(ii) EUR 12 700 000 for Spain;
(iii) EUR 5 000 000 for Italy;
(iv) EUR 2 650 000 for Portugal;
(v) EUR 31 200 000 for the United Kingdom.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic animal sampled;
(ii) EUR 0,2 per rose bengal test;
(iii) EUR 0,4 per complement fixation test;
(iv) EUR 10 per bacteriological test;
(v) EUR 1 per domestic animal vaccinated;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State referred to in paragraph 1 for the cost of the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes and shall on average not exceed EUR 50 per animal slaughtered; and
(c) shall not exceed the following:
(i) EUR 2 050 000 for Greece;
(ii) EUR 8 700 000 for Spain;
(iii) EUR 3 700 000 for Italy;
(iv) EUR 190 000 for Cyprus;
(v) EUR 1 950 000 for Portugal.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic animal sampled;
(ii) EUR 1 per domestic animal vaccinated;
(iii) EUR 2 per ELISA test;
(iv) EUR 10 per PCR test;
(v) EUR 10 per virological test;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State referred to in paragraph 1 for:
(i) the cost of carrying out laboratory tests for entomological surveillance;
(ii) the purchase of traps; and
(c) shall not exceed the following:
(i) EUR 360 000 for Belgium;
(ii) EUR 15 000 for Bulgaria;
(iii) EUR 40 000 for the Czech Republic;
(iv) EUR 80 000 for Germany;
(v) EUR 10 000 for Estonia;
(vi) EUR 40 000 for Ireland;
(vii) EUR 100 000 for Greece;
(viii) EUR 1 000 000 for Spain;
(ix) EUR 1 700 000 for France;
(x) EUR 400 000 for Italy;
(xi) EUR 20 000 for Latvia;
(xii) EUR 10 000 for Lithuania;
(xiii) EUR 10 000 for Luxembourg;
(xiv) EUR 30 000 for Hungary;
(xv) EUR 10 000 for Malta;
(xvi) EUR 40 000 for the Netherlands;
(xvii) EUR 10 000 for Austria;
(xviii) EUR 50 000 for Poland;
(xix) EUR 2 350 000 for Portugal;
(xx) EUR 100 000 for Romania;
(xxi) EUR 40 000 for Slovenia;
(xxii) EUR 50 000 for Slovakia;
(xxiii) EUR 10 000 for Finland;
(xxiv) EUR 10 000 for Sweden.
2. The programmes for the control of certain zoonotic salmonella in broiler flocks of Gallus gallus and in flocks of turkeys (Meleagris gallopavo) submitted by Poland is hereby approved for the period from 1 January 2012 to 31 December 2012.
3. The financial contribution by the Union:
(a) shall include a lump sum of EUR 0,5 per official sample taken;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State referred to in paragraph 1 and 2 for the cost of:
(i) carrying out bacteriological and serotyping tests in the framework of official sampling;
(ii) carrying out bacteriological tests to verify the efficiency of disinfection;
(iii) carrying out tests for the detection of antimicrobials or bacterial growth inhibitory effect in tissues from birds from flocks tested for salmonella;
(iv) the purchase of vaccine doses;
(v) the compensation to be paid to owners for the value of:
—
the culled breeding and laying birds of Gallus gallus,
—
the culled breeding turkey birds of Meleagris gallopavo,
—
the destroyed eggs as referred to in paragraph 4; and
(c) shall not exceed the following:
(i) EUR 1 300 000 for Belgium;
(ii) EUR 60 000 for Bulgaria;
(iii) EUR 1 500 000 for the Czech Republic;
(iv) EUR 250 000 for Denmark;
(v) EUR 1 000 000 for Germany;
(vi) EUR 30 000 for Estonia;
(vii) EUR 300 000 for Ireland;
(viii) EUR 1 000 000 for Greece;
(ix) EUR 1 000 000 for Spain;
(x) EUR 1 300 000 for France;
(xi) EUR 700 000 for Italy;
(xii) EUR 100 000 for Cyprus;
(xiii) EUR 130 000 for Latvia;
(xiv) EUR 10 000 for Luxembourg;
(xv) EUR 2 000 000 for Hungary;
(xvi) EUR 150 000 for Malta;
(xvii) EUR 3 000 000 for the Netherlands;
(xviii) EUR 800 000 for Austria;
(xix) EUR 500 000 for Poland;
(xx) EUR 200 000 for Portugal;
(xxi) EUR 200 000 for Romania;
(xxii) EUR 70 000 for Slovenia;
(xxiii) EUR 600 000 for Slovakia;
(xxiv) EUR 75 000 for the United Kingdom.
4. The maximum of the costs to be reimbursed to the Member States for the programmes referred to in paragraphs 1 and 2 shall on average not exceed:
(a) for a bacteriological test (cultivation/isolation):
EUR 7 per test;
(b) for the purchase of vaccine:
EUR 0,05 per dose;
(c) for serotyping of relevant isolates of salmonella spp.:
EUR 20 per test;
(d) for a bacteriological test to verify the efficiency of disinfection of poultry houses after depopulation of a salmonella-positive flock:
EUR 5 per test;
(e) for a test for the detection of antimicrobials or bacterial growth inhibitory effect in tissues from birds from flocks tested for salmonella:
EUR 5 per test;
(f) for the compensation to be paid to owners for the value of:
(i) a parent breeding bird of Gallus gallus culled:
EUR 4 per bird;
(ii) a commercial laying bird of Gallus gallus culled:
EUR 2,20 per bird;
(iii) a parent breeding turkey bird of Meleagris gallopavo culled:
EUR 12 per bird;
(iv) hatching eggs of parent breeding Gallus gallus:
EUR 0,20 per hatching egg destroyed;
(v) table eggs of Gallus gallus:
EUR 0,04 per table egg destroyed;
(vi) hatching eggs of parent breeding Meleagris gallopavo:
EUR 0,40 per hatching egg destroyed.
(a) Classical swine fever submitted by Bulgaria, Germany, France, Luxembourg, Hungary, Romania, Slovenia and Slovakia are hereby approved for the period from 1 January 2012 to 31 December 2012;
(b) African swine fever submitted by Italy is hereby approved for the period from 1 January 2012 to 31 December 2012.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic pig sampled;
(ii) EUR 5 per wild boar sampled;
(iii) EUR 1 per bait/vaccine;
(iv) EUR 2 per ELISA test;
(v) EUR 10 per PCR test;
(vi) EUR 10 per virological test;
(b) shall not exceed the following:
(i) EUR 210 000 for Bulgaria;
(ii) EUR 1 300 000 for Germany;
(iii) EUR 260 000 for France;
(iv) EUR 100 000 for Italy;
(v) EUR 10 000 for Luxembourg;
(vi) EUR 340 000 for Hungary;
(vii) EUR 900 000 for Romania;
(viii) EUR 30 000 for Slovenia;
(ix) EUR 500 000 for Slovakia.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per domestic pig sampled;
(ii) EUR 2 per ELISA test;
(iii) EUR 4 per seroneutralisation test;
(iv) EUR 10 per PCR test;
(v) EUR 10 per virological test;
(b) shall not exceed EUR 900 000.
2. The financial contribution by the Union:
(a) shall consist of a lump sum compensating for all costs incurred to perform the following activities and/or tests:
(i) EUR 0,5 per sample from poultry flocks;
(ii) EUR 5 per wild bird sampled in the framework of the passive surveillance;
(iii) EUR 1 per ELISA test;
(iv) EUR 1 per agar gel immune diffusion test;
(b) shall be at the rate of 50 % of the costs to be incurred by each Member State for the costs of carrying out laboratory tests other than those foreseen in point (a); and
(c) shall not exceed the following:
(i) EUR 40 000 for Belgium;
(ii) EUR 40 000 for Bulgaria;
(iii) EUR 30 000 for the Czech Republic;
(iv) EUR 40 000 for Denmark;
(v) EUR 80 000 for Germany;
(vi) EUR 10 000 for Estonia;
(vii) EUR 60 000 for Ireland;
(viii) EUR 10 000 for Greece;
(ix) EUR 90 000 for Spain;
(x) EUR 130 000 for France;
(xi) EUR 800 000 for Italy;
(xii) EUR 10 000 for Cyprus;
(xiii) EUR 20 000 for Latvia;
(xiv) EUR 10 000 for Lithuania;
(xv) EUR 10 000 for Luxembourg;
(xvi) EUR 130 000 for Hungary;
(xvii) EUR 10 000 for Malta;
(xviii) EUR 190 000 for the Netherlands;
(xix) EUR 50 000 for Austria;
(xx) EUR 100 000 for Poland;
(xxi) EUR 20 000 for Portugal;
(xxii) EUR 250 000 for Romania;
(xxiii) EUR 30 000 for Slovenia;
(xxiv) EUR 20 000 for Slovakia;
(xxv) EUR 10 000 for Finland;
(xxvi) EUR 40 000 for Sweden;
(xxvii) EUR 100 000 for the United Kingdom.
3. The maximum of the costs to be reimbursed to the Member States for the tests covered by the programmes shall on average not exceed:
(a) HI test for H5/H7:
EUR 12 per test;
(b) virus isolation test:
EUR 40 per test;
(c) PCR test:
EUR 20 per test.
2. The financial contribution by the Union:
(a) shall consist of a lump sum of:
(i) EUR 8,5 per test, compensating for all costs incurred to perform rapid tests, to fulfil the requirements of Article 12 paragraph 2 and Annex III Chapter A Part I to Regulation (EC) No 999/2001 or used as confirmatory tests in accordance with Annex X, Chapter C to the same Regulation;
(ii) EUR 15 per test, compensating for all costs incurred to perform rapid tests to fulfil the requirements of Article 12 paragraph 2, Annex III Chapter A Part II points 1 to 5 and Annex VII to Regulation (EC) No 999/2001;
(iii) EUR 4 per test, compensating for all costs incurred to perform genotyping tests;
(iv) EUR 120 per test, compensating for all costs incurred to perform primary molecular discriminatory tests as referred to in point 3.2(c)(i) of Chapter C of Annex X to Regulation (EC) No 999/2001; and
(v) EUR 25 per test, compensating for all costs incurred to perform confirmatory tests, other than rapid tests, as referred to in Annex X Chapter C to Regulation (EC) No 999/2001;
(b) shall be at the rate of 50 % of the cost incurred by each Member State for the compensation to be paid to owners for the value of their animals culled and destroyed in accordance with their BSE and scrapie eradication programmes;
(c) shall not exceed the following:
(i) EUR 1 220 000 for Belgium;
(ii) EUR 500 000 for Bulgaria;
(iii) EUR 590 000 for the Czech Republic;
(iv) EUR 730 000 for Denmark;
(v) EUR 7 690 000 for Germany;
(vi) EUR 120 000 for Estonia;
(vii) EUR 2 890 000 for Ireland;
(viii) EUR 1 540 000 for Greece;
(ix) EUR 4 320 000 for Spain;
(x) EUR 12 310 000 for France;
(xi) EUR 4 160 000 for Italy;
(xii) EUR 1 910 000 for Cyprus;
(xiii) EUR 220 000 for Latvia;
(xiv) EUR 420 000 for Lithuania;
(xv) EUR 80 000 for Luxembourg;
(xvi) EUR 1 000 000 for Hungary;
(xvii) EUR 20 000 for Malta;
(xviii) EUR 2 080 000 for the Netherlands;
(xix) EUR 1 410 000 for Austria;
(xx) EUR 2 690 000 for Poland;
(xxi) EUR 970 000 for Portugal;
(xxii) EUR 930 000 for Romania;
(xxiii) EUR 210 000 for Slovenia;
(xxiv) EUR 380 000 for Slovakia;
(xxv) EUR 350 000 for Finland;
(xxvi) EUR 500 000 for Sweden;
(xxvii) EUR 5 000 000 for the United Kingdom.
3. The maximum of the costs to be reimbursed to the Member States for the programmes referred to in paragraph 1 shall on average not exceed:
(a) for culled and destroyed bovine animals:
EUR 500 per animal;
(b) for culled and destroyed sheep or goats:
EUR 70 per animal.
2. The financial contribution by the Union:
(a) shall include a lump sum of EUR 5 per wild animal sampled;
(b) shall be at the rate of 75 % of the costs to be incurred by each Member State referred to in paragraph 1 for the cost of:
(i) carrying out laboratory tests for the detection of rabies antigen or antibodies;
(ii) the isolation and characterisation of rabies virus;
(iii) the detection of biomarker and the titration of vaccine baits;
(iv) the purchase and distribution of oral vaccine plus baits;
(v) the purchase and administration of parenteral vaccines to grazing animals; and
(c) shall not exceed the following:
(i) EUR 1 540 000 for Bulgaria;
(ii) EUR 620 000 for Estonia;
(iii) EUR 1 160 000 for Hungary;
(iv) EUR 9 270 000 for Poland;
(v) EUR 4 000 000 for Romania;
(vi) EUR 540 000 for Slovakia.
3. The maximum of the costs to be reimbursed to the Member States for the programmes referred to in paragraph 1 shall on average not exceed:
(a) for a serological test:
EUR 12 per test;
(b) for a test to detect tetracycline in bone:
EUR 12 per test;
(c) for a fluorescent antibody test (FAT):
EUR 18 per test;
(d) for the purchase of oral vaccine plus baits:
EUR 0,60 per dose;
(e) for the distribution of oral vaccine plus baits:
EUR 0,35 per dose;
(f) for the purchase of parenteral vaccine:
EUR 1 per dose;
(g) for the administration of rabies vaccines to grazing animals:
EUR 1,50 per animal vaccinated, regardless of the number of doses used.
4. Notwithstanding paragraph 2 points (a) and (b) and paragraph 3, for the part of the Polish programme that will be implemented outside its territory, the financial contribution by the Union shall:
(a) be granted only for the costs of the purchase and of the distribution of oral vaccine plus baits;
(b) be at the rate of 100 %; and
(c) not exceed EUR 1 260 000.
5. The maximum of the costs to be reimbursed for the costs referred to in paragraph 4 shall on average not exceed for the purchase and the distribution of oral vaccine plus baits EUR 0,95 per dose.
2. The second year of the multiannual programmes for the eradication of rabies submitted by Italy and Latvia is hereby approved for the period from 1 January 2012 to 31 December 2012.
3. The third year of the multiannual programmes for the eradication of rabies submitted by Lithuania and Austria is hereby approved for the period from 1 January 2012 to 31 December 2012.
4. The fifth year of the multiannual programme for the eradication of rabies submitted by Slovenia is hereby approved for the period from 1 January 2012 to 31 December 2012.
5. The financial contribution by the Union:
(a) shall include a lump sum of EUR 5 per wild animal sampled;
(b) shall be at the rate of 75 % of the costs to be incurred by each Member State referred to in paragraph 1 to 4 for the cost of:
(i) carrying out laboratory tests for the detection of rabies antigen or antibodies;
(ii) the isolation and characterisation of rabies virus;
(iii) the detection of biomarker and the titration of vaccine baits;
(iv) the purchase and distribution of oral vaccine plus baits;
(v) the purchase and administration of parenteral vaccines to grazing animals; and
(c) shall not exceed the following for the year 2012:
(i) EUR 1 600 000 for Italy;
(ii) EUR 1 700 000 for Latvia;
(iii) EUR 2 900 000 for Lithuania;
(iv) EUR 190 000 for Austria;
(v) EUR 810 000 for Slovenia;
(vi) EUR 360 000 for Finland.
6. The maximum of the costs to be reimbursed to the Member States for the programmes referred to in paragraph 1 shall on average not exceed:
(a) for a serological test:
EUR 12 per test;
(b) for a test to detect tetracycline in bone:
EUR 12 per test;
(c) for a fluorescent antibody test (FAT):
EUR 18 per test;
(d) for the purchase of oral vaccine plus baits:
EUR 0,60 per dose;
(e) for the distribution of oral vaccine plus baits:
EUR 0,35 per dose;
(f) for the purchase of parenteral vaccine:
EUR 1 per dose;
(g) for the administration of rabies vaccines to grazing animals:
EUR 1,50 per animal vaccinated, regardless of the number of doses used.
7. Notwithstanding paragraph 5 points (a) and (b) and paragraph 6, for the parts of the Latvian, Lithuanian and Finnish multiannual programmes that will be implemented outside these Member States’ territories, the financial contribution by the Union shall:
(a) be granted only for the costs for the purchase and the distribution of oral vaccine plus baits;
(b) be at the rate of 100 %; and
(c) not exceed for the year 2012:
(i) EUR 520 000 for Latvia;
(ii) EUR 1 260 000 for Lithuania;
(iii) EUR 80 000 for Finland.
8. The maximum of the costs to be reimbursed for the costs referred to in paragraph 7 shall on average not exceed for the purchase and the distribution of oral vaccine plus baits EUR 0,95 per dose.
2. The financial contribution by the Union:
(a) shall include a lump sum of EUR 0,5 per official sample taken;
(b) shall be at the rate of 50 % of the costs to be incurred by Poland referred to in paragraph 1 for the cost of the same measures as in paragraph 3 of Article 5. The maximum financial contribution for the measures set out in Article 5 by the Union shall not exceed EUR 2 500 000 for 2012.
3. The maximum of the costs to be reimbursed to Poland for the programmes referred to in paragraph 1 shall not exceed those set out in paragraph 4 of Article 5.
2. Only costs incurred in the carrying out of the annual or multiannual programmes referred to in Articles 1 to 12 and paid before the submission of the final report by the Member States shall be eligible for co-financing by means of a financial contribution by the Union.
3. In order to receive the lump sum fixed in Articles 1 to 12 in its entirety Member States shall confirm that they paid all costs incurred in the performance of the activity or test and that none of the costs have been borne by a third party, other than a Competent Authority. If part of the costs has been borne by a third party, Member States shall indicate the percentage or proportion of the total costs borne by that third party. The lump sum paid shall be reduced accordingly.
4. Notwithstanding the provisions of paragraph 2, for the costs referred to in Articles 10(4) and 11(7), the Commission, upon the request of the concerned Member State, shall pay an advance of up to 60 % of the specified maximum amount within the three months following the receipt of the request.
(a) the slaughter or culling of the animal;
(b) the destruction of the products; or
(c) the presentation of the completed claim by the owner.
2. Article 9(1), (2) and (3) of Commission Regulation (EC) No 883/2006 (11) shall apply to compensation payments made after the period 90 days referred to in paragraph 1 of this Article.
2. Where the expenditure of a Member State is in a currency other than the euro, the Member State concerned shall convert it into euro by applying the most recent exchange rate set by the European Central Bank prior to the first day of the month in which the application is submitted by the Member State.
(a) implement the programmes in accordance with the relevant provisions of Union law, including rules on competition and on the award of public contracts;
(b) bring into force by 1 January 2012 at the latest the laws, regulations and administrative provisions necessary for implementing the programmes;
(c) forward to the Commission by 31 July 2012 at the latest, the intermediate technical and financial reports for the programmes, in accordance with Article 27(7)(a) of Decision 2009/470/EC, covering the period from 1 January 2012 to 30 June 2012;
(d) only for the programmes referred to in Article 8, report to the Commission the positive and negative results of investigations detected during their surveillance of poultry and wild birds through the Commission online system, every six months, in accordance with Article 4 of Commission Decision 2010/367/EU (12);
(e) forward an annual detailed technical report to the Commission for the programmes in accordance with Article 27(7)(b) of Decision 2009/470/EC by 30 April 2013 at the latest on the technical execution of the programme concerned accompanied by justifying evidence as to the costs paid by the Member State and the results attained during the period from 1 January 2012 to 31 December 2012;
(f) implement the programmes efficiently;
(g) do not submit further requests for other contributions from the Union for those measures, and have not previously submitted such requests.
2. Where a Member State does not comply with paragraph 1, the Commission may reduce the financial contribution by the Union having regard to the nature and gravity of the infringement, and to the financial loss for the Union.
(1) OJ L 155, 18.6.2009, p. 30.
(2) OJ L 115, 29.4.2008, p. 44.
(3) OJ L 147, 31.5.2001, p. 1.
(4) OJ L 10, 14.1.2006, p. 16.
(5) OJ L 314, 1.12.2007, p. 29.
(6) OJ L 322, 2.12.2008, p. 39.
(7) OJ L 317, 3.12.2009, p. 36.
(8) OJ L 309, 25.11.2010, p. 18.
(9) OJ L 248, 16.9.2002, p. 1.
(10) OJ L 209, 11.8.2005, p. 1.
(11) OJ L 171, 23.6.2006, p. 1.
(12) OJ L 166, 1.7.2010, p. 22.
(1) OJ L 155, 18.6.2009, p. 30.
(2) OJ L 115, 29.4.2008, p. 44.
(3) OJ L 147, 31.5.2001, p. 1.
(4) OJ L 10, 14.1.2006, p. 16.
(5) OJ L 314, 1.12.2007, p. 29.
(6) OJ L 322, 2.12.2008, p. 39.
(7) OJ L 317, 3.12.2009, p. 36.
(8) OJ L 309, 25.11.2010, p. 18.
(9) OJ L 248, 16.9.2002, p. 1.
(10) OJ L 209, 11.8.2005, p. 1.
(11) OJ L 171, 23.6.2006, p. 1.
(12) OJ L 166, 1.7.2010, p. 22.
ELI: http://data.europa.eu/eli/dec_impl/2011/807/oj