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Document 02013D0722-20151209

Consolidated text: Commission Implementing Decision of 29 November 2013 approving annual and multiannual programmes and the financial contribution from the Union for the eradication, control and monitoring of certain animal diseases and zoonoses presented by the Member States for 2014 and the following years (notified under document C(2013) 8417) (2013/722/EU)

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ELI: http://data.europa.eu/eli/dec_impl/2013/722/2015-12-09

02013D0722 — EN — 09.12.2015 — 002.001

This text is meant purely as a documentation tool and has no legal effect. The Union's institutions do not assume any liability for its contents. The authentic versions of the relevant acts, including their preambles, are those published in the Official Journal of the European Union and available in EUR-Lex. Those official texts are directly accessible through the links embedded in this document

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COMMISSION IMPLEMENTING DECISION

of 29 November 2013

approving annual and multiannual programmes and the financial contribution from the Union for the eradication, control and monitoring of certain animal diseases and zoonoses presented by the Member States for 2014 and the following years

(notified under document C(2013) 8417)

(2013/722/EU)

(OJ L 328 7.12.2013, p. 101)

Amended by:

 

 

Official Journal

  No

page

date

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COMMISSION IMPLEMENTING DECISION  of 16 December 2014

  L 363

173

18.12.2014

►M2

COMMISSION IMPLEMENTING DECISION (EU) 2015/2291 of 7 December 2015

  L 323

27

9.12.2015



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COMMISSION IMPLEMENTING DECISION

of 29 November 2013

approving annual and multiannual programmes and the financial contribution from the Union for the eradication, control and monitoring of certain animal diseases and zoonoses presented by the Member States for 2014 and the following years

(notified under document C(2013) 8417)

(2013/722/EU)



CHAPTER I

Article 1

Definitions

For the purposes of the present Implementing Decision the following definitions shall apply:

(a)

sampling of domestic animals : the procedure of collecting biological material from animals at the holding by or on behalf of the Competent Authority for laboratory testing;

(b)

sampling of poultry flocks : The collection of samples from the environment of a poultry flock performed by or on behalf of the Competent Authority in the framework of a programme for the control of certain zoonotic Salmonella;

(c)

test : the procedure performed on a sample in a laboratory to detect, diagnose or evaluate disease agent presence or absence, disease process or the susceptibility to a specific disease agent;

(d)

tuberculin testing : The procedure of performing a tuberculin skin test as defined in Annex B point 2 to Council Directive 64/432/EEC ( 8 ), in the framework of a bovine tuberculosis programme.

Article 2

Bovine brucellosis

1.  
The programmes for the eradication of bovine brucellosis submitted by Spain, Croatia, Italy, Portugal and the United Kingdom are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  

The financial contribution by the Union:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(a) and 4(a) of Annex I for:

(i) 

the sampling of domestic animals;

(ii) 

rose bengal tests;

(iii) 

complement fixation tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for:

(i) 

SAT tests up to a maximum of EUR 0,25 on average per test;

(ii) 

ELISA tests up to a maximum of EUR 0,5 on average per test;

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(iii) 

bacteriological/PCR tests up to a maximum of EUR 10 on average per test;

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(iv) 

purchase of vaccines up to a maximum of EUR 0,50 on average per dose;

(v) 

the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes up to a maximum of EUR 375 on average per animal;

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(c) 

shall not exceed the following:

(i) 

EUR 5 100 000 for Spain;

(ii) 

EUR 150 000 for Croatia;

(iii) 

EUR 2 715 000 for Italy;

(iv) 

EUR 805 000 for Portugal;

(v) 

EUR 1 560 000 for the United Kingdom.

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Article 3

Bovine tuberculosis

1.  
The programmes for the eradication of bovine tuberculosis submitted by Ireland, Spain, Croatia, Italy, Portugal and the United Kingdom are hereby approved for the period from 1 January 2014 to 31 December 2014.

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2.  

The financial contribution by the Union to the Member States referred to in paragraph 1:

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(a) 

shall be at a rate of 50 % of the unit cost defined in points 3 and 4(b) of Annex I for:

(i) 

tuberculin testing;

(ii) 

gamma-interferon tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for the cost of:

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(i) 

bacteriological/PCR tests up to a maximum of EUR 10 on average per test;

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(ii) 

the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes up to a maximum of EUR 375 on average per animal;

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(c) 

shall not exceed the following:

(i) 

EUR 12 700 000 for Ireland;

(ii) 

EUR 14 000 000 for Spain;

(iii) 

EUR 330 000 for Croatia;

(iv) 

EUR 5 100 000 for Italy;

(v) 

EUR 1 035 000 for Portugal;

(vi) 

EUR 31 000 000 for the United Kingdom.

3.  
By derogation to Article 3(2), when the costs of the tuberculin testing are not directly incurred by the Member State, the financial contribution by the Union shall be limited to 50 % of the real costs incurred by the Member State for the purchase of tuberculin.

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Article 4

Ovine and caprine brucellosis

1.  
The programmes for the eradication of ovine and caprine brucellosis submitted by Greece, Spain, Croatia, Italy, Cyprus, and Portugal are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  

The financial contribution by the Union to the Member States referred to in paragraph 1, except for Greece:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(b) and 4(c) of Annex I for:

(i) 

the sampling of domestic animals;

(ii) 

rose bengal tests;

(iii) 

complement fixation tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for:

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(i) 

bacteriological/PCR tests up to a maximum of EUR 10 on average per test;

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(ii) 

the purchase of vaccines up to a maximum of EUR 0,50 on average per dose;

(iii) 

the compensation to be paid to owners for the value of their animals slaughtered subject to those programmes up to a maximum of EUR 50 on average per animal;

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(c) 

shall not exceed the following:

(i) 

EUR 7 300 000 for Spain;

(ii) 

EUR 385 000 for Croatia;

(iii) 

EUR 3 935 000 for Italy;

(iv) 

EUR 160 000 for Cyprus;

(v) 

EUR 1 125 000 for Portugal.

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3.  

The financial contribution by the Union for Greece:

(a) 

shall be at a rate of 75 % of the unit cost defined in points 4(c) of Annex I for:

(i) 

rose bengal tests;

(ii) 

complement fixation tests;

(b) 

shall be at a rate of 75 % of the eligible costs to be incurred for:

(i) 

bacteriological tests up to a maximum of EUR 15 on average per test;

(ii) 

the purchase of vaccines up to a maximum of EUR 0,75 on average per dose;

(iii) 

the remuneration of private practitioners performing vaccination and sampling activities under the programme;

(iv) 

the salaries of seasonal staff specially recruited for management of data on the implementation of the measures of that programme;

(c) 

shall be at a rate of 50 % of the eligible costs to be incurred for the compensation to be paid to owners for the value of its animals slaughtered subject to that programme up to a maximum of EUR 50 on average per animal; and

(d) 

shall not exceed EUR 3 290 000 .

Article 5

Bluetongue in endemic or high risk areas

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1.  
The programmes for the eradication and monitoring of bluetongue in domestic animals submitted by Belgium, Bulgaria, Germany, Estonia, Greece, Spain, France, Italy, Latvia, Lithuania, Malta, Austria, Poland, Portugal, Romania, Slovenia, Slovakia, and Finland are hereby approved for the period from 1 January 2014 to 31 December 2014.

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2.  

The financial contribution by the Union:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(c) and 4(d) of Annex I for:

(i) 

the sampling of domestic animals;

(ii) 

ELISA tests;

(iii) 

PCR tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for the purchase of vaccines up to a maximum of EUR 0,50 on average per dose;

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(c) 

shall not exceed the following:

(i) 

EUR 11 000 for Belgium;

(ii) 

EUR 100 000 for Bulgaria;

(iii) 

EUR 72 000 for Germany;

(iv) 

EUR 3 000 for Estonia;

(v) 

EUR 75 000 for Greece;

(vi) 

EUR 850 000 for Spain;

(vii) 

EUR 170 000 for France;

(viii) 

EUR 2 150 000 for Italy;

(ix) 

EUR 6 000 for Latvia;

(x) 

EUR 8 000 for Lithuania;

(xi) 

EUR 5 000 for Malta;

(xii) 

EUR 5 000 for Austria;

(xiii) 

EUR 25 000 for Poland;

(xiv) 

EUR 155 000 for Portugal;

(xv) 

EUR 115 000 for Romania;

(xvi) 

EUR 16 000 for Slovenia;

(xvii) 

EUR 25 000 for Slovakia;

(xviii) 

EUR 5 000 for Finland.

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Article 6

Zoonotic Salmonella

1.  
The annual programmes for the control of certain zoonotic Salmonella in breeding, laying and broiler flocks of Gallus gallus and in flocks of turkeys (Meleagris gallopavo) submitted by Bulgaria, Denmark, Germany, Estonia, Ireland, Greece, France, Croatia, Italy, Cyprus, Latvia, Luxembourg, Hungary, Malta, the Netherlands, Austria, Portugal, Romania, Slovenia, Slovakia and the United Kingdom are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  
The annual programme for the control of certain zoonotic Salmonella in flocks of turkeys (Meleagris gallopavo) submitted by Poland is hereby approved for the period from 1 January 2014 to 31 December 2014.
3.  
The annual programme for the control of certain zoonotic Salmonella in breeding flocks of Gallus gallus submitted by the Czech Republic is hereby approved for the period from 1 January 2014 to 31 December 2014.
4.  
The multiannual programmes for the control of certain zoonotic Salmonella in laying and broiler flocks of Gallus gallus and in flocks of turkeys (Meleagris gallopavo) submitted by the Czech Republic are hereby approved for the period from 1 January 2014 to 31 December 2016.
5.  
The multiannual programme for the control of certain zoonotic Salmonella in breeding, laying and broiler flocks of Gallus gallus and in flocks of turkeys (Meleagris gallopavo) submitted by the Spain is hereby approved for the period from 1 January 2014 to 31 December 2016.
6.  
The multiannual programme for the control of certain zoonotic Salmonella in breeding, laying and broiler flocks of Gallus gallus submitted by Poland is hereby approved for the period from 1 January 2014 to 31 December 2016.
7.  
The multiannual programme for the control of certain zoonotic Salmonella in breeding and laying flocks of Gallus gallus submitted by Belgium is hereby approved for the period from 1 January 2014 to 31 December 2019.
8.  

The financial contribution by the Union for the year 2014:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 2 and 4(e) of Annex I for:

(i) 

the sampling of poultry flocks;

(ii) 

bacteriological tests;

(iii) 

serotyping tests;

(iv) 

tests to verify the efficacy of disinfection;

(v) 

tests for the detection of antimicrobials;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraphs 1 to 7 for:

(i) 

purchase of vaccine up to a maximum of EUR 0,05 on average per dose;

(ii) 

the compensation to be paid to owners for the value of:

— 
the culled breeding birds of Gallus gallus up to a maximum of EUR 4 on average per bird,
— 
the culled laying birds of Gallus gallus up to a maximum of EUR 2,20 on average per bird,
— 
the culled parent breeding turkey birds of Meleagris gallopavo up to a maximum of EUR 12 on average per bird,
— 
the destroyed hatching eggs of parent breeding Gallus gallus up to a maximum of EUR 0,20 on average per egg,
— 
the destroyed table eggs of Gallus gallus up to a maximum of EUR 0,04 on average per egg,
— 
the destroyed hatching eggs of parent breeding Meleagris gallopavo up to a maximum of EUR 0,40 on average per egg;

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(c) 

shall not exceed the following:

(i) 

EUR 1 000 000 for Belgium;

(ii) 

EUR 70 000 for Bulgaria;

(iii) 

EUR 175 000 for the programme of the Czech Republic referred to in paragraph 3;

(iv) 

EUR 710 000 for the programme of the Czech Republic referred to in paragraph 4;

(v) 

EUR 320 000 for Denmark;

(vi) 

EUR 980 000 for Germany;

(vii) 

EUR 10 000 for Estonia;

(viii) 

EUR 25 000 for Ireland;

(ix) 

EUR 860 000 for Greece;

(x) 

EUR 1 390 000 for Spain;

(xi) 

EUR 1 360 000 for France;

(xii) 

EUR 205 000 for Croatia;

(xiii) 

EUR 1 700 000 for Italy;

(xiv) 

EUR 95 000 for Cyprus;

(xv) 

EUR 75 000 for Latvia;

(xvi) 

EUR 10 000 for Luxembourg;

(xvii) 

EUR 1 940 000 for Hungary;

(xviii) 

EUR 20 000 for Malta;

(xix) 

EUR 2 880 000 for the Netherlands;

(xx) 

EUR 1 190 000 for Austria;

(xxi) 

EUR 20 000 for the programme of Poland referred to in paragraph 2;

(xxii) 

EUR 3 180 000 for the programme of Poland referred to in paragraph 6;

(xxiii) 

EUR 35 000 for Portugal;

(xxiv) 

EUR 250 000 for Romania;

(xxv) 

EUR 35 000 for Slovenia;

(xxvi) 

EUR 2 500 000 for Slovakia;

(xxvii) 

EUR 150 000 for the United Kingdom.

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Article 7

Classical swine fever

1.  
The programmes for the control and monitoring of Classical swine fever submitted by Bulgaria, Germany, France, Croatia, Latvia, Hungary, Romania and Slovakia are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  

The financial contribution by the Union:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(d) and 4(f) of Annex I for:

(i) 

the sampling of domestic animals;

(ii) 

ELISA tests;

(iii) 

PCR tests;

(iv) 

virological tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for:

(i) 

the delivery of wild boars to the authorities for laboratory testing up to a maximum of EUR 5 on average per animal;

(ii) 

the purchase of oral vaccines up to a maximum of EUR 0,50 on average per dose;

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(c) 

shall not exceed the following:

(i) 

EUR 150 000 for Bulgaria;

(ii) 

EUR 710 000 for Germany;

(iii) 

EUR 35 000 for France;

(iv) 

EUR 145 000 for Croatia;

(v) 

EUR 170 000 for Latvia;

(vi) 

EUR 60 000 for Hungary;

(vii) 

EUR 835 000 for Romania;

(viii) 

EUR 485 000 for Slovakia.

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Article 8

Swine vesicular disease

1.  
The programme for the eradication of swine vesicular disease submitted by Italy is hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  

The financial contribution by the Union:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(e) of Annex I for the sampling of domestic animals;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by Italy for:

(i) 

ELISA tests up to a maximum of EUR 1 on average per test;

(ii) 

PCR tests up to a maximum of EUR 5 on average per test;

(iii) 

virological tests up to a maximum of EUR 10 on average per test;

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(c) 

shall not exceed EUR 815 000 for Italy.

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Article 9

Avian influenza in poultry and wild birds

1.  
The annual surveillance programmes for avian influenza in poultry and wild birds submitted by Belgium, Bulgaria, Denmark, Germany, Estonia, Ireland, Greece, Spain, France, Croatia, Italy, Cyprus, Latvia, Lithuania, Luxembourg, Hungary, Malta, Austria, Portugal, Romania, Slovenia, Slovakia, Finland, Sweden and the United Kingdom are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  
The multiannual surveillance programmes for avian influenza in poultry and wild birds submitted by the Czech Republic and Poland are hereby approved for the period from 1 January 2014 to 31 December 2016.
3.  
The multiannual surveillance programme for avian influenza in poultry and wild birds submitted by the Netherlands is hereby approved for the period from 1 January 2014 to 31 December 2017.
4.  

The financial contribution by the Union for the year 2014:

(a) 

shall be at a rate of 50 % of the unit cost defined in points 1(f) and 4(g) of Annex I for:

(i) 

the sampling of domestic birds;

(ii) 

ELISA tests;

(iii) 

agar gel immune diffusion tests;

(iv) 

HI test for H5/H7;

(v) 

virus isolation tests;

(vi) 

PCR tests;

(b) 

shall be at a rate of 50 % of the eligible costs to be incurred by each Member State referred to in paragraphs 1 to 3 for the delivery of wild birds to the authorities for laboratory testing in the framework of passive surveillance up to a maximum of EUR 5 on average per bird;

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(c) 

shall not exceed the following:

(i) 

EUR 50 000 for Belgium;

(ii) 

EUR 15 000 for Bulgaria;

(iii) 

EUR 15 000 for the Czech Republic;

(iv) 

EUR 65 000 for Germany;

(v) 

EUR 5 000 for Estonia;

(vi) 

EUR 70 000 for Ireland;

(vii) 

EUR 15 000 for Greece;

(viii) 

EUR 65 000 for Spain;

(ix) 

EUR 120 000 for France;

(x) 

EUR 40 000 for Croatia;

(xi) 

EUR 1 115 000 for Italy;

(xii) 

EUR 20 000 for Cyprus;

(xiii) 

EUR 20 000 for Latvia;

(xiv) 

EUR 10 000 for Lithuania;

(xv) 

EUR 10 000 for Luxembourg;

(xvi) 

EUR 165 000 for Hungary;

(xvii) 

EUR 5 000 for Malta;

(xviii) 

EUR 160 000 for the Netherlands;

(xix) 

EUR 25 000 for Austria;

(xx) 

EUR 95 000 for Poland;

(xxi) 

EUR 25 000 for Portugal;

(xxii) 

EUR 165 000 for Romania;

(xxiii) 

EUR 45 000 for Slovenia;

(xxiv) 

EUR 25 000 for Slovakia;

(xxv) 

EUR 40 000 for Finland;

(xxvi) 

EUR 30 000 for Sweden;

(xxvii) 

EUR 140 000 for the United Kingdom.

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Article 10

Transmissible spongiform encephalopathies

1.  
The programmes for the monitoring and eradication of certain transmissible spongiform encephalopathies (TSE), submitted by Belgium, Bulgaria, the Czech Republic, Denmark, Germany, Estonia, Ireland, Spain, France, Croatia, Italy, Cyprus, Latvia, Lithuania, Hungary, Malta, the Netherlands, Austria, Poland, Portugal, Romania, Slovenia, Slovakia, Finland and Sweden are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  
The multiannual programmes for the monitoring and eradication of certain transmissible spongiform encephalopathies, submitted by Greece and Luxembourg are hereby approved for the period from 1 January 2014 to 31 December 2015.
3.  
The multiannual programme for the monitoring and eradication of certain transmissible spongiform encephalopathies, submitted by the United Kingdom is hereby approved for the period from 1 January 2014 to 31 December 2018.
4.  

The financial contribution by the Union:

(a) 

shall be at a rate of 100 % of the unit cost defined in point 4(h) of Annex I for:

(i) 

rapid tests on bovine animals, performed to fulfil the requirements of Article 12 paragraph 2 and Annex III Chapter A Part I points 2.1 and 3 to Regulation (EC) No 999/2001;

(ii) 

rapid tests on bovine animals performed to fulfil the requirements of Annex III Chapter A Part I points 2.2 to Regulation (EC) No 999/2001, under the programmes of Bulgaria, Croatia and Romania or under the programmes of other Member States referred to in paragraphs 1 to 3 on bovine animals originating from Member States not included in the Annex to Commission Decision 2009/719/EC ( 9 ) or third countries;

(iii) 

rapid tests on ovine and caprine animals:

— 
in accordance with the requirements of Article 12 paragraph 2, Annex III Chapter A Part II point 5 and Annex VII to Regulation (EC) No 999/2001,
— 
up to the number necessary to fulfil the minimum requirements of Annex III Chapter A Part II points 2 and 3;
(iv) 

primary molecular discriminatory tests to perform as referred to in point 3(2)(c)(i) of Chapter C of Annex X to Regulation (EC) No 999/2001;

(b) 

shall be at a rate of 75 % of the unit cost defined in point 4(h) of Annex I for rapid tests on bovine animals, performed to fulfil the requirements of Annex III Chapter A Part I point 2.2 to Regulation (EC) No 999/2001, not falling under paragraph (a)(ii);

(c) 

shall be at a rate of 100 % of the eligible costs to be incurred by each Member State referred to paragraphs 1 to 3 for:

(i) 

confirmatory tests, other than rapid tests, as referred to in Annex X Chapter C to Regulation (EC) No 999/2001 up to a maximum of EUR 50 on average per test;

(ii) 

genotyping tests up to a maximum of EUR 6 on average per test;

(d) 

shall be at a rate of 50 % of the cost incurred by each Member State for the compensation of the owners of animals:

— 
bovines culled and destroyed up to a maximum of EUR 500 on average per animal,
— 
sheep and goats culled and destroyed up to a maximum of EUR 70 on average per animal,
— 
sheep and goats compulsorily slaughtered in accordance with Annex VII, Chapter B, point 2.2.2(b) and (c) to Regulation (EC) No 999/2001 up to a maximum of EUR 50 on average per animal; and

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(e) 

shall not exceed the following:

(i) 

EUR 260 000 for Belgium;

(ii) 

EUR 330 000 for Bulgaria;

(iii) 

EUR 165 000 for the Czech Republic;

(iv) 

EUR 2 390 000 for Germany;

(v) 

EUR 45 000 for Estonia;

(vi) 

EUR 755 000 for Ireland;

(vii) 

EUR 1 355 000 for Greece;

(viii) 

EUR 1 525 000 for Spain;

(ix) 

EUR 7 700 000 for France;

(x) 

EUR 2 115 000 for Italy;

(xi) 

EUR 300 000 for Croatia;

(xii) 

EUR 815 000 for Cyprus;

(xiii) 

EUR 65 000 for Latvia;

(xiv) 

EUR 75 000 for Lithuania;

(xv) 

EUR 30 000 for Luxembourg;

(xvi) 

EUR 660 000 for Hungary;

(xvii) 

EUR 15 000 for Malta;

(xviii) 

EUR 465 000 for the Netherlands;

(xix) 

EUR 175 000 for Austria;

(xx) 

EUR 1 220 000 for Poland;

(xxi) 

EUR 475 000 for Portugal;

(xxii) 

EUR 1 060 000 for Romania;

(xxiii) 

EUR 115 000 for Slovenia;

(xxiv) 

EUR 170 000 for Slovakia;

(xxv) 

EUR 100 000 for Finland;

(xxvi) 

EUR 105 000 for Sweden;

(xxvii) 

EUR 1 475 000 for the United Kingdom.

▼B

Article 11

Rabies

1.  
The annual programmes for the eradication of rabies submitted by Bulgaria, Estonia, Italy, Lithuania, Hungary, Poland, Romania and Slovakia are hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  
The multiannual programme for the eradication of rabies submitted by Greece is hereby approved for the period from 1 January 2014 to 31 December 2015.
3.  
The multiannual programmes for the eradication of rabies submitted by Latvia and Finland are hereby approved for the period from 1 January 2014 to 31 December 2016.
4.  
The multiannual programme for the eradication of rabies submitted by Croatia is hereby approved for the period from 1 January 2014 to 31 December 2018.
5.  
The multiannual programme for the eradication of rabies submitted by Slovenia is hereby approved for the period from 1 January 2014 to 31 December 2019.
6.  

The financial contribution by the Union for the year 2014:

(a) 

shall be at a rate of 75 % of the unit cost defined in point 4(i) of Annex I for:

(i) 

fluorescent antibody tests (FAT);

(ii) 

serological tests;

(b) 

shall be at a rate of 75 % of the eligible costs to be incurred by each Member State referred to in paragraph 1 for:

(i) 

the delivery of wild animals to the authorities for laboratory testing up to a maximum of EUR 10 on average per animal;

(ii) 

tests for the detection of biomarker up to a maximum of EUR 7,50 on average per test;

(iii) 

the isolation and characterisation of rabies virus up to a maximum of EUR 30 on average per investigation;

(iv) 

the titration of the virus contained a sample of vaccine baits up to a maximum of EUR 75 on average per sample of vaccine baits tested;

(v) 

the purchase of oral vaccine baits up to a maximum of EUR 0,60 on average per bait;

(vi) 

the distribution of oral vaccine baits up to a maximum of 0,35 on average per bait;

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(c) 

shall not exceed the following:

(i) 

EUR 1 665 000 for Bulgaria;

(ii) 

EUR 1 300 000 for Greece;

(iii) 

EUR 460 000 for Estonia;

(iv) 

EUR 140 000 for Italy;

(v) 

EUR 1 400 000 for Croatia;

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(vi) 

EUR 800 000 for Latvia;

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(vii) 

EUR 2 350 000 for Lithuania;

(viii) 

EUR 1 970 000 for Hungary;

(ix) 

EUR 6 400 000 for Poland;

(x) 

EUR 3 000 000 for Romania;

(xi) 

EUR 810 000 for Slovenia;

(xii) 

EUR 285 000 for Slovakia;

(xiii) 

EUR 250 000 for Finland.

▼B

7.  

Notwithstanding paragraphs 6 (a) and (b), for the part of the Estonian, Latvian, Lithuanian, Polish and Finnish programmes that will be implemented outside these Member States’ territories, the financial contribution by the Union for the year 2014 shall:

(a) 

be granted only for the eligible costs of the purchase and of the distribution of oral vaccine baits;

(b) 

be at the rate of 100 %; and

▼M1

(c) 

not exceed:

(i) 

EUR 110 000 for the part of the Estonian programme implemented in the Russian Federation;

(ii) 

EUR 400 000 for the part of the Latvian programme implemented in Belarus;

(iii) 

EUR 1 110 000 for the part of the Lithuanian programme implemented in Belarus;

(iv) 

EUR 1 500 000 for the part of the Polish programme implemented in Ukraine;

(v) 

EUR 95 000 for the part of the Finnish programme implemented in the Russian Federation.

▼B

8.  
The maximum of the eligible 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 baits EUR 0,95 on average per dose.
9.  

Notwithstanding the provisions of Article 13(2) for the programmes referred to under the current article:

(a) 

the Commission, upon the request of the concerned Member State, may pay an advance of up to 60 % of the specified maximum amount within the 3 months following the receipt of the request;

(b) 

eligible costs referred to in paragraph 7 shall be eligible if paid by the authorities of the third country in the territory of which the activities have been implemented and a final report and payment request has been submitted to the concerned Member State.

Article 12

African swine fever

1.  
A financial contribution to Italy for the implementation of reinforced control measures in ports and airports of Sardinia for the prevention of the spread of African swine fever is hereby approved for the period from 1 January 2014 to 31 December 2014.
2.  

The financial contribution by the Union:

(a) 

shall be at a rate of 50 % of the eligible costs to be incurred by Italy for the implementation of the measures referred to in paragraph 1;

(b) 

shall not exceed EUR 50 000 .

CHAPTER II

GENERAL AND FINAL PROVISIONS

Article 13

1.  

The financial contribution by the Union provided for in Articles 2 to 11, shall be the proportion specified in those Articles of:

(a) 

the unit costs as set for each programme in Annex I;

(b) 

eligible costs limited to the costs set out in Annex II.

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2.  
Only costs incurred in carrying out the annual or multiannual programmes referred to Articles 2 to 12 and paid before the submission of the final report by the Member State shall be eligible for co-financing by means of a financial contribution by the Union with the exception of costs referred to in Article 11(7).

▼B

Article 14

1.  
The expenditure submitted by the Member States for a financial contribution by the Union shall be expressed in euro and shall exclude value added tax and all other taxes.
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.

Article 15

1.  

The financial contribution by the Union for the annual and multiannual programmes referred to in Articles 2 to 12 shall be granted provided that the Member States concerned:

(a) 

implement the activities and measures as described in the programmes approved;

(b) 

implement the programmes in accordance with the relevant provisions of Union law, including rules on the marketing authorisation of veterinary medicinal products and rules on competition and on the award of public contracts;

(c) 

bring into force by 1 January 2014 at the latest the laws, regulations and administrative provisions necessary for actually fully implementing the programmes as of the 1 January 2014;

(d) 

forward to the Commission, the intermediate technical and financial reports for the programmes, in accordance with Article 27(7)(a) of Decision 2009/470/EC and Article 3 of Commission Decision 2008/940/EC ( 10 );

(e) 

forward an annual detailed report to the Commission for the programmes in accordance with Article 27(7)(b) of Decision 2009/470/EC and Article 4 of Decision 2008/940/EC;

(f) 

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.

Article 16

This Decision constitutes a financing decision in the meaning of Article 84 of the Financial Regulation.

Article 17

This financing decision is subject to the availability of the appropriations provided for in the draft budget for 2014 after the adoption of the budget for 2014 by the budgetary authority or if the budget is not adopted as provided for in the system of provisional twelfths.

Article 18

This Decision shall apply from 1 January 2014.

Article 19

This Decision is addressed to the Member States.



ANNEX I

UNIT COSTS

(referred to in Article 13(1)(a))

Unit costs referred to in Articles 2 to 11 are set as follows:

1. 

Sampling of domestic animals or birds:

(a) 

bovine brucellosis:



(in EUR)

Member State

Unit cost

Croatia

Portugal

0,76

Spain

1,80

Italy

United Kingdom

2,97

(b) 

ovine and caprine brucellosis:



(in EUR)

Member State

Unit cost

Croatia

Portugal

0,55

Spain

Cyprus

1,28

Italy

2,12

(c) 

bluetongue in endemic and high risk areas:



(in EUR)

Member State

Unit cost

Bulgaria

Estonia

Greece

Latvia

Lithuania

Poland

Portugal

Romania

Slovakia

Malta

0,55

Spain

Slovenia

1,28

Belgium

France

Italy

2,12

Germany

Austria

Finland

2,78

(d) 

classical swine fever:



(in EUR)

Member State

Unit cost

Bulgaria

Croatia

Hungary

Latvia

Romania

Slovakia

0,55

France

2,12

Germany

2,78

(e) 

swine vesicular disease:



(in EUR)

Member State

Unit cost

Italy

2,12

(f) 

avian influenza:



(in EUR)

Member State

Unit cost

Bulgaria

Czech republic

Estonia

Greece

Croatia

Hungary

Latvia

Lithuania

Poland

Portugal

Romania

Slovakia

Malta

1,19

Spain

Cyprus

Slovenia

2,81

Belgium

Ireland

France

Italy

United Kingdom

4,65

Denmark

Germany

Luxembourg

Austria

The Netherlands

Finland

Sweden

6,09

2. 

Sampling of poultry flocks in the framework of zoonotic Salmonella programmes:



(in EUR)

Member State

Unit cost

Bulgaria

Czech republic

Estonia

Greece

Croatia

Hungary

Latvia

Poland

Portugal

Romania

Slovakia

Malta

5,97

Spain

Cyprus

Slovenia

14,03

Belgium

Ireland

France

Italy

United Kingdom

23,24

Denmark

Germany

Luxembourg

Austria

The Netherlands

30,43

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3. 

Tuberculin testing under the bovine tuberculosis programmes:



(in EUR)

Member State

Unit cost

Croatia

Portugal

1,12

Spain

2,63

Ireland

Italy

United Kingdom

4,36

▼B

4. 

Laboratory tests:

(a) 

bovine brucellosis:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

rose bengal test

0,47

complement fixation test

0,49

(b) 

bovine tuberculosis:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

gamma-interferon test

10,43

(c) 

ovine and caprine brucellosis:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

rose bengal test

0,24

complement fixation test

0,63

(d) 

bluetongue:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

PCR test

25,08

ELISA test

1,69

(e) 

zoonotic Salmonella:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

Bacteriological test

18,19

Serotyping test

38,38

test to verify the efficacy of disinfection

16,72

test for the detection of antimicrobials

3,43

(f) 

classical swine fever:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

ELISA test

3,38

PCR test

19,01

virological test

24,95

(g) 

avian influenza in poultry and wild birds:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

ELISA test

3,26

agar gel immunodiffusion test

1,80

HI test for H5/H7

9,64

virus isolation test

37,87

PCR test

19,74

(h) 

transmissible spongiform encephalopathies:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

rapid test

7,40

discriminatory test

194

(i) 

rabies:



(in EUR)

Member State

Laboratory test

Unit cost

All Member States

fluorescent antibody test (FAT)

13,09

serological test

15,24



ANNEX II

ELIGIBLE COSTS

(referred to in Article 13(1)(b))

1.   Tests:

(a) 

the purchase of test kits, reagents and all consumables identifiable and especially used for carrying out the laboratory test;

(b) 

personnel, whatever the status, specifically allocated entirely or in part for carrying out the tests in the premises of the laboratory; the costs are limited to actual salaries plus social security charges and other statutory costs included in the remuneration); and

(c) 

overheads equal to 7 % of the sum of the costs referred to in (a) and (b) for the coordination of activities and office supplies.

2.

Compensation to owners for the value of their animals or birds slaughtered or culled, destroyed eggs and heat treated non-incubated hatching eggs:

(a) 

the compensation shall not exceed the market value of the animal immediately before it was slaughtered or culled or of the eggs immediately before their destruction or heat treatment;

(b) 

for slaughtered animals or birds and for heat treated non incubated hatching eggs, the salvage value, if any, shall be deducted from the compensation;

(c) 

the compensation to be paid to owners for the value of the animals culled or slaughtered, of the destroyed products and heat treated non-incubated hatching eggs shall be granted within 90 days from the date of:

(i) 

the slaughter or culling of the animal;

(ii) 

the destruction or the heat treatment of the products; or

(iii) 

the presentation of the completed claim by the owner;

(d) 

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.

3.

The purchase of vaccines or vaccine baits for domestic or wild animals respectively:

— 
the cost of acquisition of the vaccine doses or vaccine baits,
— 
the cost of storage of the vaccine doses or vaccine baits.

4.

 The distribution of vaccines baits for wild animals:
(a) 

the transport of the vaccines baits;

(b) 

the costs for the aerial or manual distribution of the vaccines plus baits;

(c) 

personnel, whatever the status, specifically allocated entirely or in part for distributing vaccine baits; the costs are limited to their actual salaries plus social security charges and other statutory costs included in the remuneration.

5.

The remuneration of private practitioners performing vaccination and sampling activities under the programme (referred to in Article 4(3)(b)(iii)):

shall be limited the amount paid to specifically contracted private practitioners for the sampling or for the vaccination of animals and defined on by the number of the animals sampled or vaccinated and/or the number of holdings visited for this purpose.

6.

The salaries of seasonal staff specifically recruited for the management of data on the implementation of the measures of that programme (referred to in Article 4(3)(b)(iv)):

shall be limited to the specified seasonal staff’s actual salaries plus social security charges and other statutory costs included in their remuneration.

7.

Delivery of wild animals to the authorities for laboratory testing (referred to in Article 7(2)(b)(i) and Article 11(6)(b)(i)):

shall be limited to the amount paid to hunters or other individuals or entities for the collection of dead wild animals (wild boar in the case of classical swine fever and all mammal species in the case of rabies) or the hunting of animals (wild boar in the case of classical swine fever and suspected wild mammals and healthy shot foxes and raccon dogs in the case of rabies) and their delivery (whole animal or specified part thereof) to the Competent Authority for performing eligible laboratory tests in the framework of the programme.

8.

Delivery of wild birds to the authorities for laboratory testing (referred to in Article 9(4)(b):

shall be limited to the amount paid to hunters or other individuals or entities for the delivery of suspect wild birds and their delivery and their delivery to the Competent Authority for performing laboratory tests in the framework of the programme.


( 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 213, 8.8.2013, p. 22.

( 6 )  OJ L 298, 26.10.2012, p. 1.

( 7 )  OJ L 362, 31.12.2012, p. 1.

( 8 )  OJ 121, 29.7.1964, p. 1977/64.

( 9 )  OJ L 256, 29.9.2009, p. 35.

( 10 )  OJ L 335, 13.12.2008, p. 61.

( 11 )  OJ L 171, 23.6.2006, p. 1.

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