What is Act No. 70 / 2025 Coll.?

Act No. 70 / 2025 Coll., amending Act No. 166 / 1999 Coll., on Veterinary Care and on the Amendment of Certain Related Laws (Veterinary Act), as amended, and other Related Laws — Act amending Act No. 166 / 1999 Coll., on Veterinary Care and the amendment of certain related laws (Veterinary Act), as amended, and other related laws.

When it became Act No. 70 / 2025 Coll. effectiveness?

Act No. 70 / 2025 Coll. became effective 01.04.2025.

Is Act No. 70 / 2025 Coll. still valid?

Yes, Act No. 70 / 2025 Coll. is still valid and effective.

Act No. 70 / 2025 Coll.

Act amending Act No. 166 / 1999 Coll., on Veterinary Care and the amendment of certain related laws (Veterinary Act), as amended, and other related laws

Valid Effective from 01.04.2025

ČÁST PRVNÍ Čl. I „§ 10c „§ 17 „§ 31 „§ 39 § 39a „§ 39b § 39c § 39d „§ 40a „§ 41a § 41b § 42a § 42b „§ 51 „§ 53e „§ 56a „§ 78 Čl. II ČÁST DRUHÁ Čl. III ČÁST TŘETÍ Čl. IV „§ 5e „§ 5f Čl. V Čl. VI ČÁST ČTVRTÁ Čl. VII ČÁST PÁTÁ Čl. VIII ČÁST ŠESTÁ Čl. IX ČÁST SEDMÁ Čl. X Čl. XI ČÁST OSMÁ Čl. XII Čl. XIII ČÁST DEVÁTÁ Čl. XIV Čl. XV ČÁST DESÁTÁ Čl. XVI ČÁST JEDENÁCTÁ Čl. XVII ČÁST DVANÁCTÁ Čl. XVIII § 13a § 13b § 13c Čl. XIX ČÁST TŘINÁCTÁ Čl. XX ČÁST ČTRNÁCTÁ Čl. XXI ČÁST PATNÁCTÁ Čl. XXII „Čl. VII ČÁST ŠESTNÁCTÁ Čl. XXIII ČÁST SEDMNÁCTÁ Čl. XXIV

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THE LAW

of 26 February 2025

amending Act No. 166 / 1999 Coll., on Veterinary Care and on the amendment of certain related laws (Veterinary Act), as amended, and other related laws

Parliament has decided on this law of the Czech Republic:

ČÁST PRVNÍ

Amendment of veterinary law

Čl. I

Act No. 21 / 2000 Coll., Act No. 21 / 2001 Coll., Act No. 76 / 2002 Coll., Act No. 64 / 2014 Coll., Act No. 20 / 2002 Coll., Act No. 21 / 2000 Coll., Act No. 21 / 2000 Coll., Act No. 21 / 2000 Coll., Act No. 102 / 2001 Coll., Act No. 76 / 2002 Coll., Act No. 64 / 2002 Coll., Act No. 250 / 2014 Coll., Act No. 20 / 2002 Coll., Act No. 21 / 2004 Coll., Act No. 18 / 2011 Coll., Act No. 444 / 2005 Coll., Act No. 48 / 2006 Coll., Act No. 20 / 2009 Coll.

1. Regulation (EU) No 576 / 2013 of the European Parliament and of the Council of 12 June 2013 on the non-commercial movement of pet animals and repealing Regulation (EC) No 998 / 2003. '; Commission Implementing Regulation (EU) No 2022 / 1646 of 23 September 2022 on uniform practical measures for the implementation of official controls on the use of pharmacologically active substances authorised as veterinary medicinal products or as feed additives and prohibited or unauthorised pharmacologically active substances and their residues, on the specific content of multiannual national control plans and on specific measures for their preparation. Commission Delegated Regulation (EU) No 2022 / 2292 of 6 September 2022 supplementing Regulation (EU) 2017 / 625 of the European Parliament and of the Council with regard to requirements for the introduction into the Union of consignments of food-producing animals and certain goods intended for human consumption, as amended. Commission Delegated Regulation (EU) 2016 / 361 of 28 November 2022 supplementing Regulation (EU) 2016 / 429 of the European Parliament and of the Council with regard to the rules for the use of certain veterinary medicinal products for the prevention and control of certain listed diseases. Commission Implementing Regulation (EU) 2023 / 594 of 16 March 2023 laying down specific measures to combat African swine fever and repealing Implementing Regulation (EU) 2021 / 605, as amended.'

2. In Article 2 (c), the words "animal by-products, derived products' are inserted after the words" animal products'.

3. In Article 2 (d), the words "or the treatment, processing or disposal of animal by-products and derived products' are inserted after the words" animal products'.

4. footnote 1 is replaced by the following:

"1b) For example, Act No. 258 / 2000 Coll., on the Protection of Public Health and on the Amendment of Certain Related Laws, as amended, Act No. 154 / 2000 Coll., on Breeding, Breeding and Registration of Animals, and on the Amendment of Certain Related Laws (Breeding Act), as amended, Act No. 246 / 1992 Coll., on the Protection of Animals against Torture, as amended, Act No. 91 / 1996 Coll., on Food and Tobacco Products and on Feed, as amended, Act No. 100 / 2004 Coll., on the Protection of Species of Wild Fauna and Flora by Regulation and on the Protection of Certain Related Acts (Act on Drugs), as amended, Act No. 110 / 1997 Coll.

5. footnote 2 shall read:

"(2) For example, Regulation (EC) No 999 / 2001 of the European Parliament and of the Council, Regulation (EC) No 178 / 2002 of the European Parliament and of the Council, Regulation (EC) No 852 / 2004 of the European Parliament and of the Council, Regulation (EC) No 853 / 2004 of the European Parliament and of the Council, Regulation (EC) No 1069 / 2009 of the European Parliament and of the Council, Regulation (EU) No 576 / 2013 of the European Parliament and of the Council, Regulation (EU) 2016 / 429."

6. in Article 3 (1) (m):

"(m) animal products

1. the products referred to in points 1.1, 1.10, 1.11, 1.12, 1.13, 1.14, 1.15, 2.1, 3.1, 3.4, 3.5, 3.6, 4.1, 5.1, 5.2, 5.3, 6., 7 and 8.1 of Annex I to Regulation (EC) No 853 / 2004 of the European Parliament and of the Council,

2. colostrum intended for human consumption;

3. blood intended for human consumption;

4. bee products intended for human consumption;

5. crocodile meat intended for human consumption;

6. insects intended for human consumption,

7. products obtained exclusively from the processing of unprocessed products referred to in points 1 to 6 which are intended for human consumption,

8. highly refined products as referred to in Section XVI of Annex III to Regulation (EC) No 853 / 2004 of the European Parliament and of the Council, '.

7. in Article 3 (1), the following points (o) and (p) are inserted after point (n):

"(o) animal by-products of animal origin as referred to in Article 3 (1) of Regulation (EC) No 1069 / 2009 of the European Parliament and of the Council,

(p) derived products derived from products as referred to in Article 3 (2) of Regulation (EC) No 1069 / 2009 of the European Parliament and of the Council, '.

Points (o) to (ll) shall be renumbered (r) to (nn).

8. in Article 3 (1) (s), the words "by this law, by special legislation4) and" shall be deleted;

9. footnote 4a reads:

Commission Regulation (EC) No 691 / 2006 of 13 July 2006 on the European Parliament and of the Council concerning the placing of plant protection products on the market and use of feed, amending Regulation (EC) No 1831 / 2003 and repealing Council Directive 79 / 373 / EEC, Commission Directive 80 / 511 / EEC, Commission Directive (EU) No 574 / 2011 of 16 June 2011 amending Annex I to Directive 2002 / 74 / EC and Commission Decision 2004 / 25 / EC and Commission Decision 2004 / 217 / EC as amended by Directive (EC) No 574 / 2011 / EC of the European Parliament and of the Council, amending Regulation (EC as regards the maximum levels of nitrates of nitrates, Regulation (EC), Regulation (EC) No 791 / 2006 / 2006 / 2006 / 2006 / EC and Regulation (EC as amended by Regulation (EC).

10. in Article 3 (1) (z), the words "feed of animal origin," shall be replaced by the words "animal by-products, derived products, feed and."

11. at the end of paragraph 1, the dot is replaced by a comma and the following points (oo) and (pp) are added:

"(oo) animal health rendering activities for the collection, collection, transport, storage, disposal and further processing, use or treatment of animal by-products and derived products, capture of animals without pan. 62) and of stray and abandoned animals 23a) and their quarantine or isolation;

(pp) the rendering undertaking of an establishment which processes animal by-products using standard or alternative processing methods, but in particular pressure sterilisation, and which in the designated territorial area (hereinafter referred to as the "seabed") is obliged to collect and transport animal by-products. ';

12. Footnote 9b:

"(9b) Regulation (EC) No 1069 / 2009 of the European Parliament and of the Council. Article 8 and Annex V to Regulation (EC) No 999 / 2001 of the European Parliament and of the Council. Commission Regulation (EU) No 142 / 2011. '

13. in Article 5 (1) (i), the words "submit them to the official veterinarian upon request" shall be inserted after the word "flight."

14. in Article 5 (3) (b):

"(b) to ensure that the persons referred to in (a) are aware of the obligations under paragraphs 11 and 12 and of the means of rapid contact by a private veterinarian,";

15. in Article 5e (5), the word "development" shall be inserted after the word "operation."

16. In Article 6 (2), the words "protection or surveillance zones or other restricted zones, as the case may be, 'are replaced by the words" restricted zones, infection zones' and the words "or those zones' are inserted after the words" those zones'.

17. in Article 6 (4) and (5):

"(4) The animal's veterinary certificate for movement must accompany the animal until its destination. The breeder from whom the animal is moved or, where appropriate, another person who moves the animal shall be required to transmit the health certificate to the breeder or operator to whose holding or establishment the animal is moved. The animal health certificate shall be kept by the breeder or operator to whose holding or establishment the animal is moved for at least 1 year from the date of issue.

(5) The breeder shall apply for the issue of the animal health certificate for the movement of the animal in writing or through the State Veterinary Administration Information System within at least 2 working days before the date of the intended movement of the animal. ';

18. in Paragraph 6 (7), the last sentence is deleted;

19. in Article 6 (8) (a):

"(a) the model veterinary certificate for the movement of the animal and the health certificate;"

20. in Article 9a (2), "[§ 3 (1) (hh)]" is replaced by "[§ 3 (1) (jj)]."

21. In Paragraph 10a, the sentence "For the purposes of this Act, organisms resistant to antimicrobial substances listed in Annex 2 thereto shall be added at the end of paragraph 1."

22. The following Section 10c is inserted after Section 10b:

„§ 10c

(1) The use of the medicinal products referred to in Article 4 of Commission Delegated Regulation (EU) 2023 / 361 for the prevention and control of the emergence and spread of dangerous diseases of category A or B, except in the cases and under the conditions set out in Part 3 of Annex I to Commission Delegated Regulation (EU) 2023 / 361, is prohibited.

(2) The use of vaccines to prevent and control dangerous diseases of category A or B is prohibited, except in the cases and under the conditions laid down in Commission Delegated Regulation (EU) 2023 / 361. The use of vaccines for the prevention and spread of Category A or B dangerous diseases and their control pursuant to Article 3 of Commission Delegated Regulation (EU) 2023 / 361 shall be authorised by the State Veterinary Administration; This Regulation shall be binding in its entirety and directly applicable in all Member States. The use of vaccines as referred to in the second sentence may also be provided for through compulsory preventive and diagnostic operations to prevent and control diseases and diseases communicable from animals to humans under Section 44 (1) (d).

(3) The central veterinary administration shall draw up and update an official vaccination plan to prevent and control the emergence and spread of Category A dangerous diseases as referred to in Article 6 of Commission Delegated Regulation (EU) 2023 / 361.

(4) In addition, vaccination against Newcastle disease in birds may be carried out in order to prevent and spread the disease in the Czech Republic, or where the conditions for or non-commercial movement of animals so require.

(5) For animals for which rabies is classified as Category B disease as referred to in the Annex to Commission Implementing Regulation (EU) 2018 / 188284, vaccination may be carried out in order to prevent and spread the disease on the territory of the Czech Republic or where the conditions for trade in or non-commercial movement of animals so require. This is without prejudice to the provisions of Sections 4 (1) (f) and 31a. '

23. In Article 13 (1), the word "measure 'shall be inserted after the word" make' and the words "or 17 'shall be added at the end of the text of the paragraph.

24. in Paragraph 13 (3):

"(3) Where the nature of the disease, the risk of its spread, the risk to human or animal health or, where appropriate, the risk of other serious harm or local conditions so require, the on-the-spot administration of the county veterinary service shall:

(a) the holding of animals susceptible to the disease in question at their housing sites and separately from animals suspected and prohibiting the movement of animals from or to the holding;

(b) the acquisition of an inventory of animals susceptible to the relevant disease on the holding and the keeping and updating of the inventory of animals which have died, infected or suspected;

(c) restrictions on the treatment of animal products, feedingstuffs of animal origin, articles, materials and substances which may be carriers of disease agents;

(d) the manner and rules of application of appropriate disinfectants to the entrances and exits from the places where animals susceptible to the disease concerned are housed, as well as to the entrances and entrances to the holding and exits and exits from the holding;

(e) the slaughter or culling of the animal for diagnostic purposes.

On-the-spot measures may be extended to the extent necessary to other locations referred to in Article 55 (1) (a) of Regulation (EU) 2016 / 429 of the European Parliament and of the Council. ';

25. In Article 15, the words "or 17 'shall be added at the end of the text of paragraph 1.

26.

„§ 17

In the event of a suspected occurrence of a dangerous disease listed in Part II of Annex No 2 to this Act, or in the event of confirmation of its occurrence, the competent authority shall, where appropriate, impose measures corresponding to its nature, gravity, its potential for spread and its control, as well as local conditions. Where necessary, the competent authority may impose emergency veterinary measures. ';

27. footnote 14e:

"14e) For example, Commission Regulation (EC) No 2073 / 2005, Commission Regulation (EU) No 37 / 2010, Commission Regulation (EU) 2019 / 1871 of 7 November 2019 on reference values for measures for unauthorised pharmacologically active substances present in foodstuffs of animal origin and repealing Decision 2005 / 34 / EC, as amended, Regulation (EC) No 396 / 2005 of the European Parliament and of the Council, Commission Regulation (EU) 2023 / 915 of 25 April 2023 on maximum levels of certain contaminants in foodstuffs and repealing Regulation (EC) No 1881 / 2006. '

28. in Paragraph 18 (1) (d), the words "identification mark 14f" shall be replaced by the words "identification mark; the health mark and identification mark shall comply with the requirements laid down in European Union14f); the identification mark affixed to animal products in the enterprise, plant or other establishment in the Czech Republic shall contain the abbreviation" EU. "'

29. In Paragraph 18, the following paragraph 6 is inserted after paragraph 5, including footnotes 94 and 95:

"(6) The official control of pesticides and contaminants shall be carried out by the State Veterinary Administration in accordance with Commission Delegated Regulation (EU) 2021 / 224494 and Commission Delegated Regulation (EU) 2022 / 93195.

(94) Commission Delegated Regulation (EU) 2021 / 2244 of 7 October 2021 supplementing Regulation (EU) 2017 / 625 of the European Parliament and of the Council with specific rules on official controls as regards sampling procedures for the determination of pesticide residues in food and feed.

95) Commission Delegated Regulation (EU) 2022 / 931 of 23 March 2022 supplementing Regulation (EU) 2017 / 625 of the European Parliament and of the Council by laying down rules for the implementation of official controls on contaminants in foodstuffs. '

Paragraph 6 shall become paragraph 7.

30. In Paragraph 19, the sentence "Medicinal products not intended for these animals may be administered to or used in these animals only under the conditions laid down by the Drug Act (96) is added at the end of paragraph 1. '.

Footnote 96 reads:

"96) Act No. 378 / 2007 Coll. '.

31. In Article 19 (2), the word "a" is replaced by the word "or" and the words "Article 115 of Regulation (EU) 2019 / 6 of the European Parliament and of the Council" shall be replaced by "the Law on medication96)."

32. in Paragraph 19 (3), the words "Additives and medicinal products" shall be replaced by "Substances" and the words "and under the conditions laid down by the implementing legislation" shall be added at the end of the text of the paragraph.

33. In Paragraph 19, the following paragraphs 7 and 8 are inserted after paragraph 6:

"(7) The central veterinary administration shall process the monitoring plan for certain substances and residues referred to in Article 3 of Commission Implementing Regulation (EU) 2022 / 1646, submit it to the Commission and carry out the other tasks set out in Commission Implementing Regulation (EU) 2022 / 1646.

(8) On official control of residues

(a) substances having a pharmacological effect which are authorised in veterinary medicinal products or as feed additives; or

(b) prohibited or unauthorised substances having a pharmacological effect

progresses State veterinary administration as referred to in Article 2 of Commission Delegated Regulation (EU) 2022 / 1644. '

Paragraphs 7 and 8 shall be renumbered paragraphs 9 and 10.

34. in Article 19 (10) (b):

"(b) requirements for the monitoring plan for certain substances and their residues."

35. in Article 20 (2) (e) and Article 27a (1) (d), the words "honey, royal jelly or beeswax" shall be replaced by the words "honey products intended for human consumption."

36. in Article 21 (2), the words "3 pieces" are replaced by the words "2 livestock units under the Government Regulation governing the conditions for implementing agri-environmental climate measures."

37. In Article 21, at the end of paragraph 4, the sentence "In the case of domestic slaughter of wild boar or their cross-breeds, the breeder shall be required to ensure that they are examined for the presence of a muscle (Trichinella) in a laboratory which has been issued an accreditation certificate for carrying out such an examination, at a State Institute for Veterinary Diagnostics (hereinafter referred to as the State Veterinary Institute) or in a laboratory which has been issued by the Regional Veterinary Administration pursuant to Article 50 (2) of the authorisation for this type of investigation. ';

38. In Paragraph 21 (5), the words "in writing or 'are deleted.

39. In Article 21, at the end of paragraph 7, the sentence "The requirements set out in the first and second sentences shall not apply in the case of domestic slaughter of farmed game referred to in paragraph 2. ';

40. In Article 21, paragraphs 8 to 10 are inserted after paragraph 7, including footnotes 97 and 98:

"(8) On the holding of origin, no more than 3 bovine animals, with the exception of bison, or not more than 3 solipeds, or not more than 6 pigs, or not more than 9 sheep or goats may be slaughtered on the same occasion, under the conditions laid down in European Union97. The slaughter on the holding shall be approved by the slaughterhouse operator in accordance with Section 22 (1) (a) of the Regional Veterinary Administration responsible for the slaughterhouse. The application shall be accompanied by an arrangement between the slaughterhouse operator and the breeder referred to in paragraph 9. In order to assess whether the conditions for approval of slaughter on the holding are fulfilled, the Regional Veterinary Administration shall seek the opinion of the Regional Veterinary Administration responsible locally for the place of slaughter, if this place is located in another territorial district.

(9) The arrangements referred to in paragraph 8 shall include:

(a) the name, approval number and address of the slaughterhouse;

(b) the name and address of the breeder;

(d) the precise identification and description of the equipment of the place or places within the same holding where stunning and bleeding will take place;

(e) the method of stunning and bleeding, including the method of loading the blood obtained;

(f) an indication of whether the removal of the stomach and intestines will be carried out at the place of slaughter; if so, a description of its implementation;

(g) the determination of the days of the week and the times in which the slaughter will take place.

(10) The slaughter referred to in paragraph 8 shall be notified by the breeder through the information system of the State Veterinary Administration to the Regional Veterinary Administration responsible for the place of slaughter at least 3 days before the place of slaughter. Where the slaughter notified in accordance with the first sentence is not carried out, the breeder shall immediately notify the Regional Veterinary Administration in the manner specified in the first sentence. The breeder shall indicate in the notification, in addition to the particulars referred to in the administrative order:

(a) the telephone number of the breeder or person authorised by him;

(b) the name, registration number and address of the breeder's holding, including a precise identification of the place of slaughter;

(d) whether the slaughter of bovine animals will be carried out using a firearm;

(e) the name and, where appropriate, the names of the competent person responsible for the slaughter;

(f) the number, type and identification numbers of the animals slaughtered,

(g) information on the food chain under European Union98).

97) Annex III, Section I Chapter VIa of Regulation (EC) No 853 / 2004 of the European Parliament and of the Council.

98) Annex II, Section III, to Regulation (EC) No 853 / 2004 of the European Parliament and of the Council. '

Paragraphs 8 to 19 shall become paragraphs 11 to 22.

(41) In Article 21 (11) of the introductory part of the provision, the words "or domestic slaughter of farmed deer" shall be replaced by the words "for domestic slaughter of large farmed game or for slaughter of bovine animals on the holding referred to in paragraph 8."

42. In Article 21, the following paragraph 12 is added after paragraph 11, including footnote 99:

"(12) The slaughter of bovine animals on the holding referred to in paragraph 8 by the use of a firearm shall be carried out in accordance with the requirements of the European Union Code for the slaughter of a firearm with a free projectile99).

(99) Point 3 of Chapter I of Annex I to Council Regulation (EC) No 1099 / 2009. ';

Paragraphs 12 to 22 shall become paragraphs 13 to 23.

43.In Article 21 (13) to (16), "8" is replaced by "11."

44. In Article 21 (17), the words "farmed game on the holding or for domestic slaughter of farmed deer 'are replaced by the words" large farmed game on the holding, for domestic slaughter of large farmed game or for slaughter of bovine animals, with the exception of buffalo, on the holding'.

45. In Article 21 (22), at the end of the first sentence, the words "and in so doing, in accordance with Commission Implementing Regulation (EU) 2015 / 1375 'shall be added.

46. in Article 21a (2) and (3), the words "and keeps a list of such persons" shall be replaced by the words "keeps a list of such persons and transmit it to the Central Veterinary Administration."

47. In Paragraph 22, at the end of paragraph 1, the dot is replaced by a comma and the following point (m) is added:

"(m) inform the Regional Veterinary Administration, through the Information System of the State Veterinary Administration, in accordance with Article 19 of Regulation (EC) No 178 / 2002 of the European Parliament and of the Council, where they have placed on the market animal products which are not health-free or unfit for human consumption.";

48. In Section 25, the word "ancillary 'is inserted after the word" sale'.

49. In Paragraph 25, the sentence "In the context of the sale of live fish at a separate point of sale, fish may be slaughtered, gutted, cut and otherwise treated at that point, provided that such activities are part of their sales. 'is added at the end of paragraph 3.

50. Paragraph 25 (4) reads:

"(4) In retail stores of foodstuffs with a corresponding range of animal products, animal by-products for petfood may be sold only if:

(a) are derived from animal products originally intended for human consumption when processed at the point of sale; and

(b) are placed on sale separately from food and labelled as intended for animal feed. "

51. in Article 25 (5) (a), the words "the sale of fish at a separate point of sale and for killing, evisceration" shall be replaced by the words "the sale of live fish at a separate point of sale and for slaughter, evisceration, cutting."

52. in Article 27a (1) (a), the words "live rabbits and live nutrition" shall be replaced by "and live rabbits."

(53) In Article 27a (1) (b), the words "fresh rabbit meat or fresh nutritional meat, originating in poultry, rabbits or nutrition" shall be replaced by "or fresh rabbit meat, originating in poultry or rabbits."

54. In § 27a (1) (c) of the introductory part of the provision, the words "and the address of the breeder" shall be replaced by the words "breeder and the address of the breeder where the eggs were produced."

55. In Article 27a (3), the sentence "The products referred to in paragraph 1 shall not be placed on the market or marketed by the consumer through mail order."

56.

Paragraphs 7 to 10 shall be renumbered paragraphs 6 to 9.

57. in Article 27a (7), "paragraph 7" is replaced by "paragraph 6."

58. In Article 27b, at the end of the text of paragraph 3, the words "and subsequently the user of the chase shall, in accordance with the instructions of the official veterinarian, ensure that it is disposed of at the rendering plant '.

59. In Article 27b, at the end of paragraph 3, the following sentence is added: "However, if the wild game caught does not pose a risk of spreading diseases, the user may ensure that it is disposed of at his own expense in the rendering plant, even without its submission to the official veterinarian. '

60. in Article 27b (5), the word "provide" is replaced by "submit."

61. In Article 27b, the following paragraphs 6 and 7 are inserted after paragraph 5, including footnote 100:

"(6) If the wild game caught does not pose a health risk according to the results of the examinations carried out by the trained person, the trained person may, instead of the declaration of the animal examination provided for in European Union100, make an entry in the list of the origin of the game accompanying the catch, duly completed and bearing the seal number for cloven-hoofed game or the serial number for small game. In this case, the trained person shall enter" WITHOUT AMENDMENT 'in the list of the origin of the game; the entry must also include the registration number of the trained person, the date of the inspection and the signature of the trained person.

(7) Where wild game caught presents a health risk according to the results of a test carried out by a trained person, the trained person

(a) shall enter the words "RISK" in the list of the origin of the game; the entry must also include the registration number of the trained person, the date of the inspection and the signature of the trained person; and

(b) transmit to the user a copy of the records referred to in paragraph 5 without undue delay.

100) Annex III, Section IV, Chapter II, point 4 (a) of Regulation (EC) No 853 / 2004 of the European Parliament and of the Council. '

Paragraphs 6 to 9 shall be renumbered paragraphs 8 to 11.

62. In § 27b (8), the text "§ 50 (3)" is replaced by "§ 50 (2)."

63.In Article 27b (9), "paragraph 6" is replaced by "paragraph 8."

Article 64 (31) reads as follows:

„§ 31

Where European Union provisions require the movement of animals to another Member State of the health certificate, the breeder or person involved in the trade in animals shall be required to request the Regional Veterinary Administration to issue the veterinary certificate within at least 2 working days before the date of the intended movement of the animals. ';

65. In Paragraph 32 (5), the words "and 58" shall be deleted and the words "and the provisions of the European Union adopted on its basis 101 shall be added at the end of the text of the paragraph."

Footnote 101 reads as follows:

"101) Commission Implementing Regulation (EU) 2019 / 1013. Commission Implementing Regulation (EU) 2019 / 1602. Commission Implementing Regulation (EU) 2019 / 1715 of 30 September 2019 laying down rules for the functioning of the system for the management of information on official controls and its system components (" the IMSOC Regulation '), as amended.'

66. in Article 34 (1), the words "2016 / 429 and" are replaced by the words "2016 / 429," and the words "and in Commission Delegated Regulation (EU) 2022 / 2292" are added at the end of the text of the paragraph.

67.In Paragraph 37 (3), "2019 / 625" is replaced by "2022 / 2292."

68. In Article 38a (1), the words ", composite products and derived products' shall be inserted after the word" products' and, at the end of the text of the paragraph, the words "and to small consignments of animal products, composite products and derived products which are sent to natural persons and are not intended for marketing, in accordance with Article 10 of Commission Delegated Regulation (EU) 2019 / 2122 '.

69. In Paragraph 38a (2), the words "animal products forming part of travellers' personal luggage intended for personal consumption or use 'are replaced by the words" products and consignments of products referred to in paragraph 1' and the words "consignment of animal products' are replaced by the words" consignment of products referred to in paragraph 1 ';

70. In Article 38a (3), the words "and Article 10 (3)" shall be inserted after the words "Article 8 (3)."

71. in Article 38b (1), the words "or other person responsible for the consignment (the exporter)" shall be inserted after the word "Exporter."

72.In Paragraph 38b (2):

"(2) The exporter shall apply for the issue of the health certificate within at least 2 working days before the date of the intended dispatch of the controlled goods. '

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Regulation Information

Citation	Act No. 70 / 2025 Coll., amending Act No. 166 / 1999 Coll., on Veterinary Care and on the Amendment of Certain Related Laws (Veterinary Act), as amended, and other Related Laws
Regulation Type	-
Author	-
Collection	Code of Laws

Date of Promulgation	19.03.2025
Effective from	01.04.2025
Effective until	-
Status	Valid

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