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In accordance with the decision of the Parliament:
The purpose of this law is to prevent and reduce the harmful effects of veterinary medicinal products on humans, animals and the environment and to promote appropriate use of medicinal products in veterinary medicine.
This law shall apply to the use of medicinal products and other substances used in the treatment of animals and equipment and articles used in veterinary medicine. The law also applies to the control of the use of these substances, equipment and articles. In addition, this law provides for veterinary access to veterinary medicinal products and for the control of veterinary medicinal products.
This law shall not apply to the Law on the protection of animals used for scientific or educational purposes (18/07/2013) Or products from which products obtained are not released for use as food or feed.
This law shall also apply to the implementation of European Union acts concerning the use of veterinary medicinal products, veterinary medicinal products and the control of residues of veterinary medicinal products, in so far as it is not provided for in any other law:
(1) laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and Directive of the European Parliament and of the Council Regulation (EC) No 470/2009 of the European Parliament and of the Council amending Regulation (EC) No 726/2004 of the European Parliament and of the Council ( MRL Regulation );
2) Commission Regulation (EC) No 1950/2006 of the European Parliament and of the Council on the establishment of a list of essential substances in equidae in accordance with Directive 2001 /82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products ( Horse-medicine regulation );
(3) Commission Regulation (EC) No 504/2008 implementing Council Directives 90 /426/EEC and 90 /427/EEC as regards methods for the identification of equidae;
(4) Regulation (EC) No 882/2004 of the European Parliament and of the Council on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules ( Control regulation );
5) Regulation (EC) No 853/2004 of the European Parliament and of the Council laying down specific hygiene rules for food of animal origin ( Regulation on the hygiene of foodstuffs );
(6) Regulation (EC) No .../... of the European Parliament and of the Council laying down health rules concerning animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation) 1069/2009.
Where reference is made to this Act, the act of the European Union refers to that act with its subsequent amendments.
What this law provides for in the European Union or the Member States of the European Union also applies to the European Economic Area and to the countries that belong to it.
The veterinary prescription for prescribing medicinal products is laid down in a law relating to the exercise of the veterinary profession (2006) . The supply of medicinal products, import, distribution, sales and other release for consumption are laid down in the (185/1987) . The control, use and accounting of medicinal products classified as drugs are also laid down in the drugs law (3703/2008) .
For the purposes of this law:
(1) With medication The use of a medicinal product or any other substance used for the treatment of animals and the device or article used for the administration of the medicinal product;
(2) Medicinal product The product or substance referred to in Article 3 of the Pharmaceutical Code;
(3) Medicinal product The medicinal product referred to in Article 4 of the Pharmaceutical Code;
(4) Medicinal product The substance referred to in Article 5 of the Pharmaceutical Code;
(5) With other material used for the treatment of animals Non-medicated animal or animal nutrition substance used for the promotion of animal health and welfare or for animal production reasons;
(6) Apparatus and equipment used in the veterinary medicinal product The instrument, equipment, material and instrument used for the administration of the medicinal product, the diagnosis of the disease, the treatment of the disease or health of the animal, or the study or regulation of the life function;
(7) The donation of the medicinal product The event in which the veterinarian provides medicinal products to the owner or holder of the animal, to another veterinarian or to the manufacturer of medicated feed;
(8) Farmed animals Means animals that are kept, bred, treated, slaughtered or collected for the production of food;
(9) Withdrawal period The minimum time after the last administration of the medicinal product, during which the meat of the slaughtered animal or any other animal from the slaughtered animal or the milk, honey or eggs produced by an animal or animal shall not be released as a food For use;
(10) Supervisory authority The Food Safety Agency, the Regional Administrative Agency, the Municipal Authority and the Agency for Safety and Development in the pharmaceutical sector;
(11) The veterinarian A person who has the right to practise in the veterinary profession in accordance with the law governing the exercise of the veterinary profession;
(12) The equine identification document The identification document or horse passport referred to in Commission Regulation (EC) No 504/2008 implementing Council Directives 90 /426/EEC and 90 /427/EEC as regards methods for the identification of equidae;
(13) On the national animal health programme Veterinary services law (765/2009) The national programme;
(14) Health care monitoring system An electronic system of the national animal health programme which records animal health information;
(15) At the place of the animals Of the animal identification system (238/2010) A place of residence.
Medicinal products and other animal treatment substances shall be used in such a way as to promote animal health and welfare. The medicine and any other substance used in animal treatment must be administered to the animal in such a way as to minimise the harm to the animal. In addition, the product used for the production animal and other animal treatment must be provided in such a way that the safety or quality of food from the animal is not unduly impaired. Furthermore, the administration of a medicinal product or any other substance used for the treatment of animals must not cause significant harm to man or the environment.
Equipment and articles used in veterinary medicine must be used in such a way that they do not cause unnecessary harm, pain or distress to the animal, and in such a way that the safety or quality of food from animals is not unduly undermined.
The Ministerial Decree of the Ministry of Agriculture and Forestry provides for more detailed provisions on the use of medicinal products, other substances used in the treatment of animals and equipment and equipment used in veterinary medicine.
The Regulation of the Council of State may prohibit the use of a medicinal product or any other animal used in the treatment of a medicinal product or a device or article used in a veterinary medicinal product to be used for a specified animal species or group of animals, if its use could endanger animals: The safety or quality of the food obtained or where its use may cause other significant harm to animals, humans or the environment, or where it is used to promote the growth or production of animals.
The Regulation of the Government of the European Parliament and of the European Parliament and of the Council establishing Community procedures for the authorisation and supervision of medicinal products for medicinal products or medicinal products for human and veterinary use and establishing a European Medicines Agency Regulation (EC) No 726/2004 (the Marketing authorisation regulation , the use of the veterinary medicinal product authorised under a non-marketing authorisation for use and the use of the medicinal product intended for human use in animals if the use of the product can cause harm to the animal, man or the environment.
Production animals of which beta-agonists, oestrogens, androgens or gestagens or gestagens or products derived thereof as food or feed, may not be exported to another Member State of the European Union or imported Country. However, the prohibition does not apply to live animals which have been given the abovementioned substances for therapeutic purposes or to regulate reproduction. The decree of the Council of State lays down more precisely the situations not covered by the prohibition.
For the reasons listed in Article 8 (1) and (2) of Article 8, the Ministry of Agriculture and Forestry also restricts the use of medicinal products or other substances used in the treatment of animals and equipment and equipment used in veterinary medicine.
In addition, the Decree of the Ministry of Agriculture and Forestry may prohibit the use of a medicinal product, provided that it obviates the detection, control or eradication of infectious diseases between animals and humans in Finland or causing difficulties in Evidence that live animals or food or products derived therefrom do not contain pathogens.
The Decree of the Ministry of Agriculture and Forestry may also prohibit the use of the immunological veterinary medicinal product if its administration to the animals is interfering with the detection, control or eradication of animal diseases in Finland or, if the disease, for which the medicinal product is Is intended, is not present in Finland.
The production animal shall be recognisable for the control of the use of medicinal products and for the control of residues of medicinal products during medication and treatment and within a period of withdrawal. Where a production animal cannot be identified with sufficient accuracy on the basis of the provisions relating to the labelling of the animal identification system or the animal species adopted pursuant thereto, the production animal or group of animals shall: Significant in the event of a medicinal product.
The Ministerial Decree of the Ministry of Agriculture and Forestry may, where appropriate, provide for an animal to be identified for identification purposes in the event of medication or compliance with the provisions adopted pursuant to this Act or the provisions adopted pursuant thereto.
An animal treated with a medicinal product or any other animal treated animal shall not be slaughtered for use as a food or as such an animal or the product derived therefrom, for use as a food, if the medicinal product or other The substance used in the handling of animals is detrimental to the safety or quality of the food from the animal.
The equine animal shall not be slaughtered for use as food if it is reported in Part II of Chapter IX of the identification document that the animal is not intended for slaughter for use as food.
The holder of the animal and the holder shall comply with the withdrawal periods prescribed for the product to be administered to the farm animal.
The animal shall be slaughtered for use as food during the withdrawal period of the veterinary medicinal product only if it complies with the requirements of Chapter I of Section I of Annex III to the Regulation on the hygiene of animal products. However, the animal shall not be slaughtered as a food or feed for use in oestrogenic, androgenic or gestagenic substances or medicinal products containing beta-agonists.
A product obtained from animals or animals may be released for use as food during the withdrawal period only if the method approved by the Food Safety Agency can reliably certify that the animal or the product does not contain any residues The maximum permitted under the legislation.
Farted fish or farmed game animals must not be released during the withdrawal period.
In order to ensure food safety or quality, the Decree of the Ministry of Agriculture and Forestry may, if necessary, provide for the timing of the treatment of wild game animals.
The veterinary surgeon shall prescribe a longer withdrawal period than prescribed by the medicinal product or the marketing authorisation Regulation if it is likely that the medicinal product is administered or administered by a veterinarian. Provide residues for longer than normal.
The veterinarian shall also, where appropriate, provide a withdrawal period for the medicinal product manufactured or administered to the producing animal.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the withdrawal periods referred to in paragraphs 1 and 2.
The veterinarian is entitled to obtain medicinal products from a pharmacy or a pharmaceutical wholesaler for veterinary or veterinary purposes.
The veterinary surgeon shall provide for the appropriate storage, storage and disposal of the medicinal products that it has acquired, as well as the storage of antiexpired medicinal products in storage.
The Decree of the Ministry of Agriculture and Forestry may provide for more detailed provisions on the purchase, storage and disposal of veterinary medicinal products.
The veterinarian is entitled to release medicinal products to the owner or holder of the animal for the treatment or further treatment of the animal, to another veterinary surgeon for use in veterinary or veterinary use, and (2011) For the manufacture of medicated feed for medicated feedingstuffs.
The veterinarian may dispose of medicinal products to the owner or holder of the animal for the treatment or further treatment of the animal or group of animals only after examination of the animal or the animals or, after having provided any other reliable information, on the need for medication. However, a veterinary surgeon may dispense medicinal products in a mass influx of animals or animals which threaten the health of animals or human beings, even if they have not carried out an examination of all animals themselves before they are released. In that case, the veterinarian shall immediately report to the regional administrative authority of its territory.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the supply of medicinal products and the conditions and conditions for the donation, the number and variety of medicinal products to be donated, and the exceptions to the requirement to examine all Animals.
In addition to the provisions laid down in Article 15, the veterinarian may dispose of medicinal products for the purposes of a national animal health programme for the holder or holder of the animal's holding in the normal range of animals or groups of animals. Health care and animal health care. The veterinarian and the owner of the animal or the holder of the animal shall have an agreement under Article 12 of the veterinary custody agreement on veterinary visits and measures at the place where the animals are held and the veterinarian's visits to the place of the animals shall be: Initiated.
In addition, the veterinarian will have to draw up a health care plan specific to the prevention of diseases, the planned medications and the targets for the use of veterinary medicinal products.
In the case of medicinal products, the donation is subject to Article 20 electronic medical records and the authorisation of the owner or holder of the animal, pursuant to which the Authority receives the information on the conclusion of the agreement with the veterinarian's owner or the veterinarian. The health plan, the existence of a health plan and the fact that health visits are carried out in accordance with this law.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the health plan referred to in paragraphs 1 to 3 and on the matters to be included in it, in the context of the use of medicinal products, of On the use targets, the frequency of veterinary medical visits to the holding, the reporting, the selection and quantity of medicinal products to be supplied, the conditions and limitations of the donation, and the medicinal products for the purpose of The conditions or restrictions associated with the use.
By way of derogation from the provisions laid down in Articles 15 and 16, the veterinarian responsible for the veterinary maintenance of the holding of the holding of the animals may be released to the owner or holder of the fur animals, fish and poultry intended for use in these animals. Veterinary medicinal products for the prevention of disease. In addition, the veterinarian may donate medicinal products to the owner or holder of the fur animals for the treatment of these animals or their symptoms. The condition that the veterinarian is to undergo regular inspection of the animals is a condition for the donation to be carried out on a regular basis, drawing up a health plan and a plan for the use of immunological and other veterinary medicinal products at the place of the animals and ensuring: The fact that the owner or the holder of the animal has the necessary skills and ability to identify the medication needs, treat medicines and administer them to the animal.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed rules on the conditions and restrictions of the use of medicinal products referred to in Article 1 (1) and the conditions and limitations of the use of medicinal products The choice and quantity of medicinal products.
The veterinary surgeon shall not donate alcoholic medicinal products which may be used for the purpose of drinking or medicinal products containing drugs within the meaning of Article 3 of the Narcotics Act. However, a veterinary surgeon may release to the owner or holder of the animal the quantity of a medicinal product containing the quantity of psychotropic substances required in accordance with the Convention on Psychotropic Substances (SopS 60/1976), when: The veterinary surgeon has himself stated that the medication is necessary and that the medicine is not available without difficulty or at reasonable time by veterinary prescription, without jeopardising the proper treatment of the animal.
The decree of the Ministry of Agriculture and Forestry may restrict the supply of a medicinal product to the owner or holder of the animal where the medicinal product can cause significant harm to animals, humans or the environment or any other significant harm. The decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the supply of a drug containing the substance referred to in paragraph 1 to the owner or holder of the animal.
The veterinary surgeon may charge, at most, the price of the medicinal products for the use and supply of medicinal products, for medicinal products and for the provision of medicinal products to pharmacies, pharmaceutical wholesalers or other veterinary medicinal products.
The owner or holder of the animal shall keep records of all medicinal products administered to the animal.
The holder of the animal or the holder to whom the veterinary medicinal product is supplied in accordance with Article 16 shall record the information on all medicinal products administered to the animal in the form of a healthcare monitoring system where such a possibility exists, or The other equivalent electronic system from which the data are transferred to the healthcare monitoring system.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the way in which records, accounting and healthcare monitoring systems, or any other data retention period are recorded in the electronic system.
The veterinary surgeon shall keep a record of its procuring, assignment, surrender and disposal of medicinal products.
The Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the way in which the book is kept, the information to be recorded and the length of the data retention period.
The pharmaceutical company, the pharmaceutical wholesaler or the pharmacist, who manufactures, distributes, distributes, imports or uses thyreostatic substances, oestrogenic, androgenic or gestagenic substances, or Beta-agonists or preparations containing these substances shall be kept records of these substances.
The Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the way in which the book is kept, the information to be recorded and the length of the data retention period.
The veterinarian shall provide the owner or the holder of the animal with a written report of the medicinal product he has supplied to the animal.
In addition, the veterinarian shall report to the animal owner or the holder of any other material or equipment used in the veterinary medicinal product or in the veterinary medicinal product to be administered to the animal or to be administered to the animal Where it can cause harm to the animal, to man or to the environment, or when the owner or holder of the animal asks for an explanation.
The veterinary surgeon shall provide the instructions for use of the medicinal product to be given to the owner or holder of the animal, information on the possible adverse effects or interactions of the medicinal product, as well as instructions for the correct storage and treatment of the medicinal product. The owner or holder of the animal or any other medicinal product providing the animal shall follow the instructions given by the veterinarian.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down detailed provisions on the information contained in the reports and instructions provided by the veterinarian referred to in paragraphs 1 to 3.
The veterinary surgeon may issue or prescribe medicinal products for equidae containing medicinal products which are not included in the list of equidae or pharmacologically active substances and their presence in foodstuffs of animal origin In Table 1 of the Annex to Commission Regulation (EU) No 37/2010 on the classification of MRLs only if there is a declaration in Part II of Chapter IX of the equine animal identification document that the equine animal described in the identification document is not: Intended for slaughter for use as food.
The veterinary surgeon shall record, in accordance with the instructions given in Chapter IX of Chapter IX of the Equidae Regulation, the equine animal identification document in accordance with the guidelines laid down in Chapter IX of Chapter IX of the Equidae Regulation. The recording shall not be required if the entry referred to in Part II of the identification document contains the entry referred to in paragraph 1.
The Decree of the Ministry of Agriculture and Forestry may provide for more detailed provisions on the obligation of a veterinarian to ensure the labelling referred to in paragraph 1 and the obligation to record the medicinal products given to the equine animal The identification document.
In addition to what is required in Section III of Annex II to the hygiene regulation for animals to be slaughtered for slaughter, the owner or the holder of the animal shall be informed in writing of: Any other body or entity receiving the animal or product from which the animal or the product obtained from the animal is released for human consumption during the withdrawal period.
The holder of the animal or the holder shall also provide a written explanation of the results of the study referred to in Article 12 (3) during the withdrawal period during the withdrawal of the medicinal product from the animal or animal released for use as food.
Where a production animal is sold or otherwise disposed of in the course of a treatment or withdrawal period, the owner or holder of the animal shall inform the purchaser or the new holder of the medicinal product administered to the animal and the date on which the medicinal product has been administered, and A withdrawal period. For farmed animals for slaughter, the information shall be indicated in the food law (2006) Or from the period covered by it.
The Ministry of Agriculture and Forestry directs and supervises the implementation and enforcement of this law and of the provisions of the European Union referred to in Article 4 of this Act and of the provisions thereof.
The Agency is planning, directing, developing and monitoring the implementation and enforcement of this law and of the provisions adopted pursuant to it.
In addition to what is provided for in this Act for the tasks of the Authority, the Agency shall:
(1) be responsible, as the competent authority, for the tasks entrusted to it by the acts of the European Union referred to in Article 4 which are covered by this law;
(2) develop monitoring of the use of antimicrobials in different animal species;
(3) maintain the information necessary for the implementation of this law on the medicinal products authorised for use in Finland and on their withdrawal periods;
(4) organise and provide training in the implementation of this law for veterinary surgeons, pharmacies, owners and holders of animals and other participants in veterinary medicinal products.
The Office shall ensure the implementation and enforcement of this law and of the provisions adopted thereunder in its territory.
The municipal veterinarian shall ensure compliance with this law and the provisions adopted pursuant to it, in accordance with the provisions of the Regional Administrative Agency, on the length of time of the animals. In order to avoid any obstacle, the Regional Administrative Agency may order the local veterinarian to carry out these tasks outside its territory.
The Agency shall monitor and supervise compliance with this law and the provisions adopted pursuant to it in pharmaceutical companies, pharmaceutical wholesalers and pharmacies.
Compliance with this law shall be subject to the provisions of the Control Regulation.
In addition to what is laid down in the Food Law for the design and implementation of national control of foreign food products, the Food Safety Agency shall draw up a A multi-annual national control programme for the control of the use and disposal of substances and equipment used in veterinary medicine. The programme shall also cover the control of prescription medicines in accordance with Article 10 of the Law on the pursuit of the veterinary profession. The programme is part of a national control plan under the Control Regulation. The programme shall be reviewed as necessary, however, at least every four years. The programme shall contain at least the following information:
(1) the objectives and the coverage of the controls;
(2) the criteria according to which the risks of different types of control are assessed and the frequency and frequency of their control is chosen;
(3) definition of the content and methods of controls;
(4) when dealing with suspicion or verification of unlawful conduct;
(5) Methods used to assess the implementation of the control programme.
The Agency shall implement the programme at national and regional level, each within its territory. The Agency may provide specific provisions for the implementation of the programme to the regional administrative agencies.
The decree of the Ministry of Agriculture and Forestry provides for more detailed provisions on the content of the control programme.
Without prejudice to the provisions of confidentiality, the Authority shall have the right to obtain, free of charge, the information and documents necessary for the performance of the duties provided for in this Act or by European Union law, and from the owners and holders of the animal, Veterinarians, pharmaceutical wholesalers, pharmacies and other actors within the meaning of this law, as well as state and municipal authorities.
The right to information shall also apply to the information necessary for the purpose of carrying out such checks, which would otherwise be kept secret by private commercial or professional activities or by private economic status or health status.
The Food Safety Agency shall have the right to carry out the duties provided for in this Act, to obtain, as agreed, a summary of the healthcare monitoring systems for the use of medicinal products.
The Authority shall have the right to carry out the checks and investigations required to carry out checks and, for that purpose, access to the premises and premises of the animals in which medicinal products, other substances used for the treatment of animals, feed and veterinary medicinal products used in veterinary medicine Storage of equipment and equipment, or information relating to animals or their medication.
In addition, the Authority shall have the right to carry out the checks and investigations required to carry out checks and inspections, as well as to the premises in which the veterinary profession, the transport, brokering or trading of animals or the Activities.
In the event of a permanent residence, an inspection may be carried out only where there is reason to suspect that the owner or the holder of the holding has committed a criminal offence punishable by a custodial sentence and an inspection or an investigation is necessary To investigate.
The supervisory authority shall allow the owner or the holder of the premises or the holder of the investigation to be present during the inspection or investigation, if the owner, the holder, or The veterinarian will be available without delay. However, the absence of the owner, holder or veterinarian of the premises shall not prevent the conduct of the inspection or investigation.
The Authority shall have the right to take, for the purposes of supervision, the quantity of animals, products thereof, animal feed and drinking water necessary for the purpose of monitoring, and the owner or holder of the animal, the veterinarian or any other The operator holding the feed, the medicinal product, any other material used for the treatment of animals or the device or article used in the veterinary medicinal product. Sampling shall be sent by the sampling probe to the national reference laboratory designated under Article 37 of the Food Law, to the official laboratory approved under the food law or to another EU Member State. To the official laboratory. The other samples shall be sent to the Food Safety Agency or to the competent laboratory. Such a laboratory must have a written quality system and be technically competent and be able to produce reliable results.
The Ministerial Decree of the Ministry of Agriculture and Forestry provides for more detailed provisions on sampling and testing and on the qualification requirements for laboratories.
What this law provides for the right of the supervisory authorities to carry out checks, to take samples, to access the places of control and to obtain the necessary information and documents for the purpose of monitoring, including in European Union legislation, or Inspectors referred to in an international agreement binding Finland where this is required by law or contract. Where appropriate, the Authority shall cooperate with the inspectors of the international authorities.
The holder, the holder of the animal, the veterinarian and any other operator referred to in this law shall, at their expense, provide the Authority and the international authority referred to in Article 37 with the necessary assistance for control and inspection. The owner or holder of the animal shall be obliged to organise the conditions under which checks and sampling can be carried out safely, taking into account the normal behaviour of the animal.
Police assistance shall be provided by the police (872/2011) .
Customs may, where appropriate, provide the Authority with professional assistance in order to control the prohibitions referred to in Article 8 (3).
The confidentiality of the information obtained under the supervision is governed by the law of the authorities (18/09/1999) And Article 7 of the Control Regulation.
Notwithstanding the obligation of professional secrecy, information obtained under the supervision of a private or Community financial position, business or professional secret or private personal circumstances may be disclosed:
(1) to the authorities for the performance of the tasks provided for in this Act or by this Act;
(2) prosecuting, police and customs authorities in order to investigate the crime; and
(3) foreign institutions and international authorities, if required by European Union law or by an international agreement which is binding on Finland.
The Regional Administrative Agency may order the killing of a production animal and its carcase and animal products to be disposed of if the animal has been authorised under this law for a medicinal product or a substance whose use is under this law. Restricted to non-authorised uses, or where a device or article prohibited under this law has been used for the treatment of an animal. The Office may also prohibit the sale of such an animal or any other donation, the slaughter of the animal as a food or feed, and the release of products from the animal for use as food or feed. In addition, the Office may prohibit the transfer of other production animals from the place of the animals during the studies and studies to be carried out.
The Office of the Regional Administrative Board may order the killing and destruction of a place other producing animal, where a medicinal product or a medicinal product prohibited under this law has been found to be prohibited under this law, The use of which is restricted by virtue of this law, and the owner or holder of the animal refuses to bear the costs arising from the studies to determine whether such medicinal product has been administered to the animal.
For the purposes of studies and studies, the Regional Administrative Agency may prohibit the movement of farm animals from the holding of animals and the donation of animal products as a food or feed, if obtained from the animal The food is found to be in excess of the maximum permitted levels.
The Office of the Regional Administrative Board may order the holding of animals of the animals and other animals held or held by the same person on a temporary basis, on a temporary basis, if, under this law, the animal or the product obtained from it has been found to: A prohibited medicinal product or a medicinal substance whose use is restricted under this law, or where there have been repeated cases of residues exceeding the permitted levels in food obtained from animals.
The Regional Administrative Agency shall make a reference to the law on the information system of the rural economy (194/2008) Prohibitions on the movement, transfer and use of the animal referred to in paragraphs 1 and 3. In addition, the Regional Administrative Agency shall record the withdrawal of the ban as soon as it can be ascertained that the prohibition is no longer justified.
The Ministerial Decree of the Ministry of Agriculture and Forestry lays down more detailed provisions on the implementation of provisions and prohibitions and enhanced surveillance.
The Regional Administrative Agency may intensify the provision referred to in Article 41 or the prohibition on the imposition of a penalty payment or, at the risk of failing, the action to be taken at the expense of the non-compliance officer.
The threat of a periodic penalty payment and the commission of a periodic penalty payment shall be laid down in the (1113/1990) .
In the cases referred to in Article 41 (1) and (2), the Office may, in the case referred to in Article 41 (1) and (2), take place in the place of the holding of animals or of the animal or any other substance or veterinary medicinal product used for the treatment of the feed, medicine or other animals. The equipment or article used, where there is reason to suspect that the feed, the medicinal product or any other substance used in the treatment of animals contains, under this law, unauthorised medicinal substances or substances whose use is restricted under this law, or That the use of the device or article in the veterinary medicinal product is Prohibited.
In addition, the regional administrative office may take over the possession of the animal or the holder, the veterinarian or any other substance held by the holder, veterinary surgeon or other animal referred to in this Act, if: Reasonable grounds for suspecting that the medicinal product or the substance was acquired or disposed of in contravention of this law or of the provisions adopted pursuant to it.
The deposit must be carried out in the presence of the witness. The owner or holder of the animal shall be issued with a certificate showing the amount of the assets taken and the reason for taking over.
For the purpose of studies, samples may be taken without compensation.
Where appropriate, the approved property may be stored at the place of the holding or by the owner, or the holder, the veterinarian or any other operator referred to in this Law, in a manner which is appropriate to the person referred to in this law, or in sealing or otherwise marked In storage.
The Regional Administrative Board shall decide how to proceed with the acquisition of property. Subscribed assets may be ordered to be destroyed if the acquired assets are found to contain medicinal substances or substances which are prohibited under this law, the use of which is restricted under this law or, if taken in veterinary medicine, The use of a device or article is prohibited under this law, or has been detected in contravention of this law or of any provisions adopted pursuant to this law. Otherwise, the property shall be ordered to be returned to its owner or holder.
Penalty report is punishable by criminal law (39/1889) Article 44 (5) .
The penalty for smuggling is regulated Article 4 of Chapter 46 of the Penal Code -In.
Every intention or carelessness
(1) use medicinal products, medicinal products or other substances used in the treatment of animals or veterinary medicinal products and equipment used in veterinary medicinal products under Articles 7 to 9, or in accordance with provisions adopted pursuant thereto, Article 16 of the MRL Regulation or Regulation 2 of the equine medicinal product , in breach of Article
(2) violate the export or import restrictions provided for in Article 8 (3) or adopted pursuant to it;
(3) neglects the obligation laid down in Article 10 to mark an animal in the context of medication;
(4) fails to comply with the obligation laid down in Article 12 to comply with the withdrawal periods for medicinal products administered to the farmed animal,
(5) disclose, acquire, store, store, store or dispose of medicinal products, substances or other substances used in the treatment of animals or in veterinary medicine, in contravention of Articles 14 to 18 or any provisions adopted pursuant thereto;
(6) fails to comply with Articles 20 to 22, or under them or in accordance with the accounting obligations laid down in Article 3 (2) of the Equidae Regulation,
(7) fails to fulfil its obligations under Articles 23 to 25 or under them; or
(8) fails to fulfil its obligations under Article 38;
Shall be condemned, unless the law provides for a heavier penalty in the rest of the law, On the violation of veterinary medicinal products Fine.
The Authority may submit to the preliminary investigation authority without notifying any infringement which must be considered to be of minor importance for the whole.
Any violation of a penalty or an obligation imposed by the penalty imposed by this law may not be punished for the same offence.
In the case of a sample taken from a production animal or a product obtained from the product, it is established that the animal has been given a medicinal product whose use is prohibited under this law or where a food obtained from an animal is found to: In excess of the maximum levels for medicinal products, the owner or holder of the animal shall pay the costs of the studies and studies carried out in order to investigate the matter, as well as the alleged infringement to the next temporary enhanced surveillance; Costs related to the studies.
Where an animal has been ordered to be killed and destroyed pursuant to Article 41, the owner or holder of the animal shall bear the costs of the killing and destruction of the animal.
Where control is found that medicinal products or other substances used in the treatment of animals are acquired, used or disposed of in contravention of this law or of any provisions adopted pursuant to it, a suspected person's owner or The costs of the additional explanations to be carried out by the holder or the veterinarian, as well as the costs of the temporary enhanced surveillance following the infringement.
More detailed provisions on the national arrangements required by Articles 27 and 28 of the Control Regulation and the quantification of the amount of fees, as well as fees related to the national control programme, shall be provided by the Ministry of Agriculture and Forestry Regulation. The criteria for payments shall take into account the provisions of the Control Regulation.
The fees referred to in paragraphs 1 and 2 shall be directly eligible. Their succession is governed by the law on the implementation of taxes and charges (20/2007) .
Article 23 of the Veterinary Service Act provides for the right of a municipality to receive compensation from State resources in accordance with this law for carrying out the duties of a municipal veterinary surgeon.
The decision of the Regional Administrative Office under this Act or of the European Union Act to be implemented by this Act shall be appealed against in the same way as the Law on Administrative Law (18/06/1996) Provides.
A decision pursuant to Articles 41, 43 and 44 of this Act may provide that, in spite of the appeal, the decision is to be complied with, unless the appeal authority decides otherwise. The appeal must be treated as a matter of urgency.
The procedure provided for by a veterinarian in breach or abuse of the right to purchase, use or dispose of medicinal products is laid down in a law relating to the exercise of the veterinary profession.
National animal health programmes shall set national targets for the use of essential veterinary medicinal products to promote controlled and appropriate use of medicinal products.
The body managing the healthcare programme shall inform the regional administrative authority of the establishment of the place of destination of the animals at the time of suspicion that the provisions of this Act and the provisions adopted pursuant thereto have not been complied with.
This Act shall enter into force on 1 December 2014.
This law repeals the law on veterinary medicine (17/1997) . The Regulations of the Ministry of Agriculture and Forestry adopted under the repealed Law remain in force.
Otherwise, any reference to the law on the treatment of animals which has been repealed by law or regulation shall be construed as referring to this law after the entry into force of this law.
THEY 98/2013 , MmVM 3/2014, EV 16/2014