Decree No. 25 / 2020 Coll.
Order on the prescription of medicinal products for veterinary care
Valid
Order
Effective from 01.02.2020
25
DECLARATION
of 22 January 2020
on the prescription of medicinal products for veterinary care
According to Article 114 (3) of Act No. 378 / 2007 Coll., on Medicines and on the Amendment of Certain Related Acts (Act on Medicines), as amended by Act No. 70 / 2013 Coll. and Act No. 262 / 2019 Coll., ("the Act '), the Ministry of Agriculture provides for the implementation of Sections 71 (2), 74 (1) and 80a (3) of the Act:
Preliminary provisions
This decree provides
(a) the extent of the data given on the recipe and the requisition, the period of validity, the restrictions with regard to the type and quantity of medicinal products for the treatment of animals that may be prescribed for them and the rules for their use;
(b) the data reported on the blue-striped recipe, its period of validity, restrictions on the type and quantity of medicinal products for the treatment of animals prescribed therein and the rules for its use;
(c) data presented on demand with a blue stripe displayed in paper form, its period of validity, restrictions on the type and quantity of medicinal products for the treatment of animals prescribed therein and the rules for its use;
(d) the manner, content and classification requirements of the Regulation for medicated feedingstuffs, the number of copies of and handling this Regulation; and
(e) the particulars of the rules for veterinary autogenic vaccines and the conditions for handling them by veterinary surgeons and manufacturers.
Prescription of medicinal products not containing highly addictive substances
Scope of data on the recipe and the requisition
(1) The recipe shall include the following information:
(a) the name and, where applicable, the name, surname, address of the place of permanent residence, or place of residence in the territory of the Czech Republic, if any, if it is a stranger, and the telephone number of the keeper of the animal, if he is a natural person; for a legal person, the name or business name, registered office and telephone number; telephone numbers shall be provided only if their users agree; If there is a breeder for whom registration is required under another legislation (1), the number of the holding where the animals for which the prescribed medicinal product is intended shall be indicated,
(b) the type of animal for which the medicinal product is prescribed; if necessary for the unambiguous identification of the animal or group of animals treated, further information necessary for such unambiguous identification shall be provided;
(c) the prescribed medicinal product:
1. the name under which the medicinal product has been authorised (2), the pharmaceutical form, the strength and the package size, or
2. the pharmaceutical name or its synonym or abbreviation given in the Czech Pharmacopoeia (3) or the name of the medicinal or auxiliary substance included in the list provided for by other legislation4), individually for all components of the medicinal product, with the simultaneous indication of the amount of individual ingredients required and the instructions for the preparation and delivery of the medicinal product in the case of the preparation of the medicinal product,
(d) the quantity of medicinal product expressed in the case of:
1. authorised medicinal products, by indication of the package size and number of packages by Roman numerals, together with its word expression in Latin,
2. the preparation of medicinal products by the number of doses of Roman numerals, together with its verbal expression in the Latin language or, where appropriate, the volume or quantity of medicinal product to be prepared,
(e) instructions on the use of the medicinal product,
(f) the word "Cascade," if it is for the prescription of a medicinal product to be used pursuant to Article 112, 113 or 114 of the Regulation on veterinary medicinal products and following those Articles in accordance with the Law on medicinal products,
(g) the word "Prophylaxis," if it is a case of prescription for an antimicrobial medicinal product to be used for prophylactic purposes,
(h) the wording "Metaphylaxis," if applicable, for the prescription of an antimicrobial medicinal product to be used for the purposes of metaphylaxis,
(i) the duration of the withdrawal period, if it is a case of prescription of the medicinal product to be used in an animal producing animal products intended for human consumption, by:
1. the word "OL - PI," if the withdrawal period laid down in accordance with the terms of its marketing authorisation is to be respected after the administration of the authorised veterinary medicinal product,
2. the word expression "OL," supplemented by the number of days or hours, for the relevant animal products expressed as "meat," "milk," "eggs" or "honey," if the conditions of point 1 are not fulfilled, or if the withdrawal period after the administration of the registered veterinary medicinal product must be extended,
3. the words "OL as instructed by the veterinarian," where it is not possible to make a clear decision on the duration of the withdrawal period at the time of issue of the recipe and the withdrawal period is determined subsequently by the veterinarian and is recorded in a dossier under the legislation governing the prescription of medicinal products for the provision of medical services (11); This form of expression may not be used where the breeder of an animal producing animal products intended for human consumption does not keep records of the use of the medicinal product in accordance with other legislation13),
(j) the date of issue;
(k) an imprint of the stamp containing the identification details of the prescribing veterinarian, the name and, where appropriate, the names and surnames, the place of business, where appropriate the place of practice, the identification number, if any, and the telephone number; where the prescribing veterinarian carries out professional veterinary activities (5) as an employee of a natural or legal person authorised to carry out professional veterinary activities, the name and, where applicable, the name and surname of the prescribing veterinarian, the name and, where appropriate, the surname, and surname, place of business and, where applicable, the place of practice of his employer, if any, the natural person, or the name, seat and identification number of his employer, if applicable, the legal person,
(l) the registration number of the Chamber of Veterinary Physicians,
(m) the signature of the prescribing veterinarian; and
(n) the words "Providing veterinary care."
(2) The following information shall be provided on the requisites:
(a) the identification of the person authorised to carry out the veterinary professional activities, the name and, where applicable, the name, surname, place of business, place of practice, identification number, if any, and the number of the prescribing veterinarian; where the veterinarian carries out professional veterinary activity (5) as an employee of a natural or legal person authorised to carry out professional veterinary activity (5), the name and, where applicable, the name, surname, place of regular veterinary care and the identification number of his employer, if any, or the name, registered office and identification number of his employer, if applicable, if the legal person,
(b) the name of the prescribed medicinal product,
1. the name under which the medicinal product has been authorised (2) or, where appropriate, the name of the active substance contained therein, the pharmaceutical form, the strength and the package size; or
2. the pharmaceutical name or its synonym or abbreviation referred to in the Czech Pharmacopoeia (3), or the name of the medicinal or auxiliary substance in the list provided for by other legislation4), individually for all components of the medicinal product, with the simultaneous indication of the quantity required in the case of the preparation of the medicinal product,
(c) the quantity of the medicinal product expressed in the case of:
1. authorised medicinal products by indication of the package size and number of packages by Roman numerals, together with their word expression in Latin; If the package size is not stated, the minimum authorised pack size for the medicinal product concerned shall be considered as prescribed,
2. the preparation of medicinal products by the number of doses of Roman numerals, together with its verbal expression in the Latin language or, where appropriate, the volume or quantity of medicinal product to be prepared,
(d) the date of issue,
(e) an imprint of the stamp containing the identification details of the prescribing veterinarian, the name and, where appropriate, the names and surnames, the place of business, where appropriate the place of practice, the identification number, if any, and the telephone number; where the prescribing veterinarian carries out professional veterinary activities (5) as an employee of a natural or legal person authorised to carry out professional veterinary activities, the name and, where applicable, the name and surname of the prescribing veterinarian, the name and, where appropriate, the surname, and surname, place of business and, where applicable, the place of practice of his employer, if any, the natural person, or the name, seat and identification number of his employer, if applicable, the legal person,
(f) the registration number of the Chamber of Veterinary Physicians, where the prescribing veterinarian is a private veterinarian under another legislation (6),
(g) the signature of the veterinarian issuing the application; and
(h) the words "Providing veterinary care."
(3) If it is about prescribing authorised veterinary medicinal products, the recipe and the need for a medicinal product may be prescribed using an international non-proprietary name recommended by the World Health Organisation, indicating the required pharmaceutical form, strength and quantity.
(4) If the dispensation of the medicinal product is to be repeated, the recipe shall contain a repeat statement of "Repetatur 'and an indication of the total number of outputs expressed in Roman numerals, together with its word expression in Latin.
(5) In the case where the dosage established by the Czech Pharmacopoeia is deliberately exceeded when prescribing a medicinal product, or when prescribing a veterinary medicinal product, the dosage or indication referred to in the Summary of Product Characteristics (7), the symbol "! 'shall be indicated; In the case of an individually prepared medicinal product, excess dosage must be written in Latin.
(6) If the veterinarian persists in issuing the prescribed medicinal product, the word "Do not confuse 'shall be given.
(7) In the event of a threat to the life of an animal in which there is a risk of delay, the veterinarian may prescribe the medicinal product without giving all the particulars referred to in paragraph 1. In such a case, the veterinarian shall provide all the particulars referred to in paragraph 1 that can be ascertained, but the recipe shall always contain at least the stamp imprint referred to in paragraph 1 (k) or any other means of unambiguous identification of the veterinarian, his handwritten signature and telephone number, the medicinal product referred to in paragraph 1 (c), its quantity and instructions on the use of the medicinal product, the type of animal, the date of issue of the recipe and the word "Acute Veterinary Care."
(8) The recipe and the requisition shall not contain any characters or elements which restrict the legibility of the data to the recipe or which would have an advertising character.
Rules on the use of recipes and requests
(1) Recipes and vouchers are stored in such a way as to prevent their loss or alienation and the possibility of their misuse.
(2) Unfilled recipes and vouchers may not be stamped or signed by a veterinarian or by a legal person authorised to carry out professional veterinary activity (5).
Duration of the recipe and request
(1) Formula prescribed
(a) antimicrobials shall be valid for 5 calendar days from the day following the day of issue;
(b) other medicinal products shall be valid for 14 calendar days from the day following the day of their issue; if there is no prescription for a prescribed medicinal product containing an addictive substance under the legislation governing the treatment of addiction8) or category 1 scheduled substance under the directly applicable European Union drug precursor regulation (9), the prescribing veterinarian may extend the validity of the prescription for a maximum period of 1 year from the date of its issue; for a prescription containing an addictive substance under the legislation governing the treatment of addiction8), or a category 1 scheduled substance under the directly applicable European Union drug precursor regulation 9), the prescribing veterinarian may extend the prescription for a maximum period of 30 days.
(2) The prescription for prescribed medicinal products to be re-dispensed is valid for a maximum period of 6 months from the day following its issue, unless otherwise specified by the prescribing veterinarian, and the prescribing veterinarian may extend the prescription for a maximum period of 1 year from the day following its issue.
(3) The recipe issued in the case of emergency veterinary care pursuant to Article 2 (7) shall be valid until the end of the first day following that of issue.
(4) The medicinal product application shall be valid for 60 days from the day following that on which it is issued.
Restrictions on the type and quantity of prescribed medicinal products
(1) No more than one type of medicinal product may be prescribed for the recipe.
(2) In accordance with the procedure laid down in Article 2 (4), a medicinal product containing an addictive substance may not be prescribed under the legislation governing the treatment of addiction8), or a scheduled substance of category 1 under the directly applicable European Union drug precursors regulation 9).
(3) In accordance with the procedure laid down in Article 2 (3), a authorised medicinal product for human use or a authorised medicinal product containing an addictive substance under the legislation governing the treatment of addiction8), or a scheduled category 1 substance under the directly applicable regulation of the European Union regulating drug precursors (9), may not be prescribed for the recipe or request.
(4) A prescription issued in the case of acute veterinary care pursuant to Article 2 (7) may not be prescribed for a medicinal product which contains an addictive substance under the legislation governing the treatment of addiction8), or for that category 1 substance under the directly applicable European Union drug precursor regulation 9).
(5) If the prescribed quantity of the medicinal product is not available in the pharmacy, the pharmacist shall issue an extract of the recipe "Extract" to the missing medicinal product. On repeated dispensing of the medicinal product, unless the latter is the case, the pharmacist shall issue an extract of the recipe which shall serve as a document for inspection on the packages issued. The extract shall be valid for 14 days from the day following its issue.
(1) The recipe on the basis of which medicinal products are to be distributed to breeders under Section 77 (1) (c) (7) of the Act cannot be re-used.
(2) Only a veterinary medicinal product which:
(a) is not a product containing antimicrobials intended for injection in accordance with the Marketing Authorisation Decision,
(b) it is not limited for its use only by a veterinarian under Article 40 (5) of the Act;
(c) it is not restricted to putting into circulation or to its use under another legislature10);
(d) is not an immunological veterinary medicinal product which contains live agents of diseases or diseases communicable from animals to humans or for preventive vaccination of animals against diseases and diseases communicable from animals to humans listed in the list of diseases and diseases communicable from animals to humans against which animals must not be preventive vaccinated (5);
(e) does not contain an addictive substance under the legislation governing the treatment of addiction8), or a scheduled substance of category 1 under the directly applicable European Union drug precursors regulation 9); or
(f) the marketing authorisation shall indicate the type of animal for which it is prescribed.
(3) A veterinary medicinal product the issue of which is subject to a prescription may be prescribed for the recipe referred to in paragraph 1 in a quantity not exceeding that which corresponds to the need for a therapeutic bark determined by the treating veterinarian for a period not exceeding 28 days. For emergency treatment, a veterinary medicinal product may be prescribed not exceeding the average weekly requirement on the holding concerned.
(4) The recipe referred to in paragraph 1, other than the particulars referred to in Paragraph 2 (1), also contains:
(a) a medical diagnosis or reason for prescribing the veterinary medicinal product; and
(b) the number of animals and the category of animals for which the veterinary medicinal product is intended.
(5) When prescribing medicinal products for the recipe referred to in paragraph 1, the prescribing veterinarian shall complete the first sheet and 2 copies. The first sheet and the first copy shall be transmitted by the prescribing veterinarian to the breeder. The second copy shall be kept by the veterinarian. The breeder shall keep the first sheet and hand the licence to the distributor when the veterinary medicinal products are delivered. The breeder, the veterinarian and the distributor shall keep the recipe or its signature in accordance with Section 9 (11) of the Act.
(6) Paragraph 4 shall apply mutatis mutandis to determine the period of validity of the recipe referred to in paragraph 1.
Prescription of medicinal products containing highly addictive substances
Prescription with blue stripe
Medicinal products that can only be issued with a blue stripe or a blue stripe recipe under the addictive law are prescribed
(a) a blue-striped recipe under Section 80a (1) (b) of the Act, with the first sheet and 2 prescription entries being completed; the first sheet and the first copy are intended for delivery of the prescribed medicinal product at the pharmacy, the second copy is left in the block of recipes used,
(b) a blue stripe request under Paragraph 80a (1) (d) of the Act, with the first sheet of the request being completed at the time of the prescription, and 3 copies; the first sheet of the application form and 2 signatures are intended for the delivery of the prescribed medicinal product at the pharmacy, the third copy is left in the block of the requested goods.
Data on the medical prescription with blue stripe
(1) The blue-striped recipe shall contain the data referred to in Article 2 (1).
(2) The blue stripe request shall show the data referred to in Article 2 (2).
Restrictions on the type and quantity of medicinal products for the treatment of animals that may be prescribed to a prescription with a blue stripe
(1) Only medicinal products for which the law on addictive substances provides can be prescribed for a blue stripe recipe or blue stripe requisition.
(2) No more than 1 type of medicinal product may be prescribed for a blue-striped recipe.
(3) A maximum of 5 types of medicinal products may be prescribed for a blue stripe.
Duration of the Blue Stripe prescription
The blue-striped recipe and the blue-striped voucher shall be valid for 14 calendar days starting on the day following the day of issue, unless otherwise specified by the veterinarian, but not more than 30 days.
Rules on the use of the Blue Stripe medical prescription
(1) For the production and distribution of medical prescription forms with a blue stripe and for the procedure in the event of their loss or theft, the conditions laid down in Section 22 of the legislation governing the prescription of medicinal products for the provision of medical services (11) shall apply mutatis mutandis, and authorised persons shall also be authorised to provide veterinary care under Section 6 (1) (d) of the Act.
(2) For the treatment of blue stripe recipes and blue stripe vouchers by authorised persons referred to in paragraph 1, the conditions laid down in Article 23 of the legislation governing the prescription of medicinal products when providing medical services (11) shall apply mutatis mutandis.
(3) For blue-striped recipes and blue-striped vouchers, the models laid down in the legislation regulating the prescription of medicinal products when providing medical services (11) shall be used.
Method, content and breakdown requirements of the Regulation for medicated feed, number of copies of and handling this Regulation
(1) Medicated feedingstuffs are prescribed for prescription containing the particulars set out in Annex V to the Regulation on medicated feedingstuffs (hereinafter referred to as the Annex),
(a) the details of the veterinarian referred to in point 1 of the Annex shall be understood as:
1. the name, names, and surnames, place of business, place of practice, identification number, if any, and telephone number; where the prescribing veterinarian carries out professional veterinary activities (5) as an employee of a natural or legal person authorised to carry out professional veterinary activities, the name and, where applicable, the name and surname of the prescribing veterinarian, the name and, where appropriate, the surname, and surname, place of business and, where applicable, the place of practice of his employer, if any, the natural person, or the name, seat and identification number of his employer, if applicable, the legal person,
2. registration number of the Chamber of Veterinary Physicians,
(b) the unique number of the Regulation referred to in point 2 of the Annex means the identification number of the person authorised to carry out the professional veterinary activities followed by the registration number of the Chamber of Veterinary Doctors prescribing the veterinarian, followed by the calendar year in which the Regulation was issued and the serial number of the Regulation in the relevant calendar year;
(c) the particulars of the breeder referred to in point 3 of the Annex shall be understood as:
1. if it is a natural person, name or surname, surname, address of the place of permanent residence or place of residence in the Czech Republic, if it is a foreigner, and telephone number, if the breeder agrees to mention it,
2. if the legal person, name or business name, registered office and telephone number are concerned, if the breeder agrees to mention it,
3. if the breeder for whom a registration obligation is laid down under another legislation (1), the number of the holding where the animals for which the medicated feed is intended are kept,
(d) for the purposes of point 7 of the Annex, the following shall apply:
1. the provisions of Paragraph 2 (1) (f) in the case of the prescription of a veterinary medicinal product pursuant to Article 112, 113 or 114 of the Regulation on veterinary medicinal products, mutatis mutandis;
2. Paragraph 2 (1) (h) in the case of the prescription of a veterinary medicinal product pursuant to Article 107 (4) of the Regulation on veterinary medicinal products, mutatis mutandis,
(e) for the purposes of point 12 of the Annex, Article 2 (1) (i) (1) or (2) shall apply mutatis mutandis.
(2) The provisions of Article 16 (8) of the Regulation on medicated feed shall apply to the validity of the Regulation on medicated feed.
(3) The prescription for medicated feed shall be drawn up by the veterinarian in 4 copies, of which 1 copy shall be retained, 1 copy transmitted to the breeder referred to in the prescription for medicated feed and 2 copies shall be transmitted to the manufacturer of the medicated feed. Where medicated feed has not been produced before the issue of the prescription for medicated feed pursuant to Article 8 of the medicated feed Regulation, the manufacturer of the medicated feed shall ensure that the production and subsequent delivery of medicated feed is carried out without undue delay upon receipt of the valid prescription for medicated feed.
(4) The manufacturer of the medicated feed shall keep 1 copy of the prescription for medicated feed and 1 copy shall be transmitted to the supplier of the medicated feed. Where the manufacturer provides the supply of medicated feed produced by him himself, he shall also keep a copy for the supplier. In addition, the manufacturer of medicated feed shall, through the information system of the State Veterinary Administration, transmit the prescription for medicated feed to the Regional Veterinary Administration, which is the locally relevant holding where medicated feed is to be used.
(5) The supplier of the medicated feed, or the manufacturer who also provides for the supply of medicated feed, shall complete the particulars referred to in point 15 of the Annex in the form of a copy of the prescription for medicated feed intended for the breeder in accordance with point 16 of the Annex when the medicated feed is delivered.
(6) The veterinarian may request the manufacturer to provide copies of the prescription for medicated feed for the purpose of their transmission in accordance with paragraphs 3 and 4; the veterinarian shall indicate this on the prescription for medicated feed. In this case, the veterinarian shall draw up only 3 copies of the prescription for medicated feed. The manufacturer shall ensure that the particulars on the copies can be read and unchanged when making copies of the prescribed medicated feed.
(7) Where the producer of medicated feed is a person established in a Member State of the European Union other than the Czech Republic and where the supply of medicated feed produced by it is provided by another supplier, the responsibility of the manufacturer for the treatment of medicated feed rules referred to in paragraph 6 may be provided by that supplier of medicated feed.
(8) The veterinarian who has issued the prescription for medicated feed and the breeder who has used the medicated feed shall keep the appropriate copies of the prescription for medicated feed for at least 5 years from the date of its issue.
Prescription of veterinary autogenic vaccines
(1) The prescription for the veterinary autogenic vaccine contains:
(a) identification of the breeder in accordance with Article 2 (1) (a);
(b) the species and category of animal for which the veterinary autogenic vaccine is intended,
(c) indication or indication of the reason for use;
(d) the identification of the antigens or pathogens from which the autogenic vaccine is to be produced;
(e) the address and registration number of the holding from which the antigens or pathogens for the production of the veterinary autogenic vaccine are to be collected; where antigens or pathogens have already been collected pursuant to Article 71 (5) of the Act, the indication of the holding and the location from which the antigens or pathogens have been collected and the date of such collection shall be given;
(f) the number of doses of the veterinary autogenic vaccine or its quantity to be produced;
(g) a special warning to be given on the packaging or package leaflet of the veterinary autogenic vaccine;
(h) the contact details of the Regional Veterinary Administration responsible for receiving the notification referred to in Article 71 (6) of the Act;
(i) the name, name, surname and place of business of the manufacturer of the veterinary autogenic vaccine, if any, if it is a natural person, or the name and address of the legal person;
(j) a stamp showing the particulars of the prescribing veterinarian referred to in Article 2 (1) (k);
(k) the registration number of the Chamber of Veterinary Physicians,
(l) the date of issue of the Regulation; and
(m) the signature of the veterinarian who issued the prescription for the veterinary autogenic vaccine.
(2) The veterinary autogenic vaccine prescription shall be issued by the competent attending veterinarian in 3 copies, of which 1 copy shall be retained and 2 copies shall be transmitted to the manufacturer of the veterinary autogenic vaccine. This manufacturer shall retain one copy and transmit one copy, using any means of data transmission, to the Regional Veterinary Administration within whose jurisdiction the veterinary autogenic vaccine will be used.
(3) The veterinarian may request the manufacturer of the veterinary autogenic vaccine to provide copies of the prescription for the veterinary autogenic vaccine for the purpose of their transmission in accordance with paragraph 2; this shall be indicated by the veterinarian on the prescription for the veterinary autogenic vaccine. In this case, the veterinarian shall draw up only 2 copies of the prescription for the veterinary autogenic vaccine. The manufacturer shall ensure that the particulars on the copies are legible and unchanged when making copies of the submitted prescription for the veterinary autogenic vaccine.
(4) The veterinarian who has issued the prescription for the veterinary autogenic vaccine shall keep it for at least 5 years from the date of its issue.
Repeal
They shall be deleted:
1. Decree No. 54 / 2008 Coll., on the method of prescribing medicinal products, the particulars given on the prescription and the rules of use of the prescription.
2. Decree No. 405 / 2008 Coll., amending Decree No. 54 / 2008 Coll., on the method of prescribing medicinal products, the data on the prescription and the rules of use of the prescription.
3. Decree No. 177 / 2010 Coll., amending Decree No. 54 / 2008 Coll., on the method of prescribing medicinal products, the data on the prescription and the rules of use of the prescription, as amended by Decree No. 405 / 2008 Coll.
4. Decree No. 190 / 2013 Coll., amending Decree No. 54 / 2008 Coll., on the method of prescribing medicinal products, the data on the prescription and the rules of use of the prescription.
5. Decree No. 413 / 2017 Coll., amending Decree No. 54 / 2008 Coll., on the method of prescribing medicinal products, the data on the prescription and the rules of use of the prescription, as amended.
Efficacy
This Decision shall enter into force on 1 February 2020.
Minister:
Ing. Toman, CSc., v. r.
1) Act No. 154 / 2000 Coll., on the breeding, breeding and registration of livestock and amending certain related laws (Breeding Act), as amended.
2) § 4 (1) of Act No. 378 / 2007 Coll.
3) § 11 (d) of Act No. 378 / 2007 Coll.
4) Decree No. 85 / 2008 Coll., establishing a list of active substances and excipients which may be used for the preparation of medicinal products.
5) Act No. 166 / 1999 Coll., on veterinary care and amending certain related laws (Veterinary Act), as amended.
7) § 3 (1) of Act No. 378 / 2007 Coll.
8) Act No. 167 / 1998 Coll., on addictive substances and amending some other laws.
9) Regulation No 273 / 2004 of the European Parliament and of the Council of 11 February 2004 on drug precursors.
10) Decree No 291 / 2003 Coll., concerning the prohibition of the administration of certain substances to animals whose products are intended for human consumption and the monitoring (monitoring) of the presence of unauthorised substances, residues and contaminants for which animal products could be harmful to human health, in animals and in their products, as amended.
11) Decree No. 329 / 2019 Coll., on the prescription of medicinal products for the provision of health services.
12) Decree No. 136 / 2004 Coll., laying down details of the marking of animals and their registration and registration of holdings and persons provided for by the Breeding Act, as amended.
13) Decree No 344 / 2008 Coll., on the use, prescription and supply of medicinal products in the provision of veterinary care, as amended by Decree No 139 / 2011 Coll.
Sign in for notes, favorites and notifications
Regulation Information
| Citation | Decree No. 25 / 2020 Coll., on the Prescription of Medicinal Products for Veterinary Care |
|---|---|
| Regulation Type | Order |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 31.01.2020 |
|---|---|
| Effective from | 01.02.2020 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
Comments 0