The increase in the trade in genetic material made it necessary, in its day, to lay down health and zootechnical rules at Community level for the purposes of animal health protection and exchange management. commercial, basic for the development of a competitive and sustainable livestock sector. However, the absence of a specific regulation at national level advises to dictate a rule that regulates the conditions for the placing on the market of genetic material.

This regulation aims to ensure the rational and safe use of these products, through the increase in the transparency of commercial transactions. As animal genetics is the first link in the production process for much of our livestock sector, the extension and consolidation of artificial insemination procedures, spermatic cryopreservation or embryo transfer are in the light of its economic development, especially in recent years.

In order to promote this development, it is necessary to guarantee the zootechnical and sanitary quality of the genetic material, for which it is contemplated the establishment of minimum conditions and registers that must formalize the responsible for the various establishments. The establishment of this common base will lead to greater harmonisation of procedures developed in these centres.

As regards the monitoring of genetic material once marketed, it would not be possible without the existence of reliable records, in particular of the collection, storage or distribution centres of the same, as well as of the ova/embryo collection teams, in which the basic data identifying them and a codification of the activities to which they are dedicated are included.

This set of actions is complemented by the establishment of a document that must accompany each consignment of genetic material, thus complying with Article 50 of Law 8/2003, of April 24, of health animal. In addition to the health requirements, it is necessary, in addition to the health requirements, to collect information of a zootechnical nature for the material derived from pure-bred animals, in order to facilitate the more efficient use of such material.

This regulation is complemented by the rules which refer to the information to be contained in the packaging containing the genetic material, which is essential to ensure its monitoring throughout the Chain of marketing and make it easier to apply correctly.

The aim is to ensure both the sanitary conditions and the zootechnical quality of the genetic material in order to be used in cattle farms, increasing the information that reaches the cattle farmer, facilitating the mission of those responsible for the improvement of each breed and allowing effective traceability of the breed. This provision also contributes to the development of the activities referred to in Royal Decree 2129/2008 of 26 December 2008 establishing the National Programme for the Conservation, Improvement and Promotion of Livestock breeds. This programme provides for the possibility of establishing exceptional measures to prevent the disappearance or elimination of genetic resources. For this reason, it is possible to provide for specific exceptions to the fulfilment of the general requirements for endangered, difficult-to-manage and/or intended for experimental purposes, studies or for germplasm.

Moreover, the present royal decree applies within Spain a series of European Union rules laying down the health rules applicable to intra-Community trade in the genetic material of sheep, bovine, Goats and swine or Equidae. In this way, the health requirements for the national movement of this material are matched to the requirements already applied for intra-Community trade. In particular, the rules applicable to intra-Community trade to be applied to domestic trade are: Council Directive 90 /429/EEC of 26 June 1990 laying down the animal health rules applicable to the Council Directive 89 /556/EEC of 25 September 1989 on animal health conditions governing the use of animal health and veterinary legislation on animal health and on imports of semen of animals of the porcine species and their amendments, Council Directive 89 /556/EEC of 25 September 1989 on animal health conditions Intra-Community trade and imports from third countries of embryos of animals Council Directive 88 /407/EEC of 14 June 1988 laying down the animal health requirements applicable to intra-Community trade in and imports of semen of the bovine species from the bovine species (bovine animals) and their amendments to the Directive Council Regulation (EEC) No 3952/88 of 21 December 1993 laying down detailed rules for the application of Council Regulation (EEC) No 4052/88 on the approximation of the laws of the Member States relating to the approximation of the laws of the Member States relating to the approximation of the laws of the Member States relating to the of animals, semen, ova and embryos not subject, in respect of these conditions, to the rules specific Community measures referred to in Section I of Annex A to Directive 90 /425/EEC and their amendments.

With this royal decree, the aforementioned Community legislation is not modified, but it is intended to apply the same one that only regulates the intra-Community movement, to a different reality, such as the exchanges within Spain, whose Regulation is a matter of internal law of the Member States and is still regulated by a 1971 rule.

This royal decree is dictated by virtue of the habilitation contained in the fifth final provision of Law 8/2003, of April 24.

In the elaboration of this standard, the autonomous communities and representative entities of the sectors affected have been consulted. It has also submitted to the procedure for information on technical standards and regulations and regulations relating to the services of the information society provided for in Directive 98 /34/EC of the European Parliament and of the European Parliament. Council of 22 June, as well as Royal Decree 1337/1999 of 31 July, which incorporates this Directive into Spanish law.

In its virtue, on the proposal of the Minister of the Environment, the Rural and Marine Environment, with the prior approval of the Minister of the Presidency, in agreement with the Council of State and after deliberation of the Council of Ministers in its June 17, 2011 meeting,

DISPONGO:

Article 1. Object and scope of application.

This royal decree is intended to:

(a) Establish basic sanitary and zootechnical standards for the collection, storage, distribution and marketing of genetic material of the bovine, ovine, caprine, porcine, and Equidae species, at national level.

b) The creation of a register for national and intra-community trade in centres and equipment dedicated to the collection, storage or distribution of genetic material.

c) The development of the identification system for the genetic material for national and intra-Community trade.

Article 2. Definitions.

1. For the purposes of this royal decree, the definitions laid down in Article 3 of Law 8/2003 of 24 April of animal health, in Article 2 of Royal Decree 2129/2008 of 26 December 2008 establishing the National programme for the conservation, improvement and promotion of livestock breeds, in Article 2 of Royal Decree No 2256/1994 of 25 November 1994 laying down the animal health requirements applicable to intra-Community trade and the imports of semen of animals of the bovine species, in Article 2 of Royal Decree 855/1992 of 10 July 1992, laying down the animal health conditions governing intra-Community trade in and imports from third countries of embryos of domestic animals of the bovine species, in Article 2 of the Royal Decree 1148/1992 of 25 September 1992 laying down the animal health requirements applicable to intra-Community trade in and imports of semen of domestic animals of the porcine species, in Article 2 of the Royal Decree 1881/1994 of 16 September 1994 laying down the animal health conditions applicable to the intra-Community trade in and imports from third countries of animals, semen, ova and embryos not subject, in respect of these conditions, to the provisions contained in Section I of Annex A to Royal Decree 1316/1992 of 30 June 1992. October.

2. In addition,

following definitions shall apply:

(a) Distributor: any duly authorised operator which has appropriate means and materials and which markets genetic material at national level from storage centres or collection of genetic material and whose recipients are the end users.

b) Marketing: making available a third of genetic material, whether for consideration or free of charge, within the national territory.

(c) Competent Authority: the bodies of the Autonomous Communities in the field of their competences.

d) heterospermic dose: seminal dose obtained from mixing the ejaculate of two or more donor males.

Article 3. Rules for the national trade in genetic material.

1. For the placing on the national market for the reproductive purposes of semen, ova and embryos of animals of the bovine, ovine, caprine and porcine species, and of Equidae, the following health conditions must be met and Zootechnical:

(a) In the case of semen of bovine animals, the conditions laid down in Article 3.1 (a), (b) and (c) of Royal Decree 2256/1994 of 25 November 1994.

(b) In the case of embryos of bovine animals:

1. Höber was obtained as a result of artificial insemination or in vitro fertilisation, with semen from a donor of semen collection centre approved by the competent authority for the collection, treatment and storage of semen, or semen imported in accordance with Article 3.1 (a) of Royal Decree 2256/1994 of 25 November 1994.

In exceptional circumstances, the competent authority of the autonomous communities, in accordance with Community rules, may authorise the exchange of embryos for certain particular breeds conceived by cover natural or bull-made by bulls whose health status complies with the provisions of Annex B to Royal Decree 2256/1994 of 25 November 1994.

2. The conditions laid down in Article 3.1 (b), (c) and (d) of Royal Decree 855/1992 of 10 July.

(c) In the case of semen of animals of the porcine species:

1. º That has been collected, treated and stored in a collection and/or storage facility authorized from the health point of view in accordance with the provisions of paragraph 1.a. of Annex IV.

2. No other than that obtained from animals of the porcine species, the health status of which complies with the requirements of paragraph 1 (b) of Annex IV.

3. º That has been collected, treated, stored and transported in accordance with paragraph 1.c) of Annex IV.

(d) In the case of semen of animals of the ovine and caprine species, and of equidae:

1. º That has been collected, treated and stored in a collection and/or storage facility authorized from the health point of view in accordance with the provisions of paragraph 2.a) of Annex IV.

In the case of ovine and caprine species, semen may also be collected and treated on a holding that meets the requirements of Royal Decree 1941/2004 of 27 September 2004 laying down the rules of the police (a) health governing intra-Community trade in and imports from third countries of ovine and caprine animals.

2. ° That has been obtained from animals whose health status complies with the requirements of paragraph 2.b) of Annex IV.

3. º That has been collected, treated, stored and transported in accordance with paragraph 2.c) of Annex IV.

e) In the case of ova and embryos of animals of the ovine, caprine, porcine, and Equidae species:

1. º That have been obtained from donor females which comply with the conditions laid down in paragraph 3 (a) of Annex IV by a collection team approved by the competent authority or which have been produced by a centre for the production of embryos authorised by the competent authority and which complies with the conditions laid down in Annex IV (3) (b).

2. º That have been collected, processed and preserved in an appropriate laboratory and stored and transported in accordance with paragraph 3.c) of Annex IV.

3. The semen used for the insemination of the donor females must be in accordance with the provisions of paragraph 2 of Annex IV in the case of ovine and caprine animals and the Equidae, whereas in the case of the porcine species shall be in accordance with the conditions laid down in paragraph 3.d) of Annex IV.

2. The placing on the market of heterospermic doses shall be permitted only when the same is marketed in the national territory only and the offspring obtained therefrom are not intended for reproduction.

3. In addition, semen, ova and embryos must:

a) Proceed from a center or team authorized by the competent authority.

(b) To be accompanied by a document containing the data specified in Part A of Annex I, issued by the official veterinarian or, where appropriate, by the authorised or authorised veterinarian. For this purpose, the competent authorities may authorise the veterinary surgeons responsible for the centre or equipment concerned, where the movement is between approved centres or equipment, and from those to holdings where the movement takes place. insemination or a distributor.

If the genetic material is to be marketed as originating from pure-bred animals, the data provided for in Part B of Annex I shall be included in that document, provided that such data cannot be obtained from a source of public consultation of associations or organisations of animal breeders of livestock breeds officially recognised for the management of the Genealogical Book of the relevant breed. In the event that such source exists and contains the required information, the referral to the source shall be sufficient.

Those documents must be kept for at least three years in order to be supervised by the competent authority.

4. In the case of genetic material from a distributor agent, it shall be covered by a commercial document containing the data necessary to ensure that traceability is ensured at all times.

5. This Article shall not apply to the genetic material obtained on the same holding in which the females to which it is intended are located, or to be moved to another holding of the same holder, with both holdings of origin and destination in the same municipal or lower territorial unit as, where applicable, the competent authority is established.

Article 4. Data logging.

1. For each approved collection centre or equipment of genetic material, an updated register shall exist, allowing at least:

(a) Identify the donor animal of the genetic material and the date of collection, as well as the batch number and doses.

b) Know the results of the genetic material assessment tests.

c) Know the destination address or registration number of the target or end user centre and the number of doses issued from the collection centre and the date of issue.

2. Each storage centre must keep an up-to-date record, which allows it to be known, at least:

(a) The identification or registration number of the source center of the stored material, the date of receipt, the donor animals of the material, and the number of units in its possession.

b) The destination address or registration number of the destination center and the number of units dispatched from the storage center and the date of dispatch.

3. Distributors must keep an up-to-date register, which allows them to know at least:

(a) The address or registration number of the home center and the number of seminal doses acquired and their date of receipt.

(b) The address or registration number of the holding of destination and the number of semi-final doses placed on the market and their date of issue.

4. Final users who use the genetic material must keep an up-to-date register, which allows to know at least the address or registration number of the centre of origin or distributor from which the genetic material used and the date of receipt.

5. Such records may be carried by electronic means and shall be kept for a minimum period of three years in order to be supervised by the competent authority.

Article 5. Identification of genetic material.

For the marketing of the genetic material, the containers containing it must be provided with a visible mark which allows the date of collection to be established by means of any of the following formats:

a) Indicating with the first two digits the year and the next three digits (AA/DDD),

b) indicating with the first two digits the day, the next two digits of the month, and the last two digits of the year (DD/MM/YY).

Followed by the identification of the animal or donor animals and the code of the collection centre or equipment, in accordance with the format referred to in Article 6.1 for the latter.

In addition, for the genetic material of the animals of the pure breeds, they must be provided with the identification of the breed according to the coding of the International Committee for animal recording-ICAR, if this is possible, or of the codification set out in Annex III in another case.

However, for the case of heterospermic doses, intended for domestic trade, the identification of the donor animals may be replaced by the heterospermic identifier code of the production centre, provided that the center has available a record of the equivalences of the heterospermatic identification code with the identification of the donor animals of the dose.

The identification of the genetic material from animals covered by the exceptions referred to in the second provision, as well as the heterospermic doses, must be carried out in accordance with the the preceding paragraphs, but preceded by a capital N, so that it is unequivocally distinguished from the rest of the genetic material.

Article 6. Registration of centers and equipment.

1. Any approved centre or equipment, dedicated to the collection, storage or distribution of genetic material, must be registered and shall have one or more codes, assigned by the competent authority, in accordance with an alphanumeric code, which will consist of:

a) A code with the letters IS, then double digits, to identify the autonomous community where the center or equipment is authorized, according to Annex II.

b) A two-letter code assigned based on the activity that is performed, according to the following correlation table:

1. Semen Collection: RS.

2. Storage Center: CA.

3. The egg/embryo collection team: ET.

4. Distributor: D.

c) Two digits to be assigned in a correlative manner, according to the record order made for the effect in the autonomous community.

d) A code composed of one or more letters, depending on the species/s with which it is intended to work, taking into account the following correlation table:

1. Bovine: B.

2. Ovina/ Caprine: PO.

3. Porcin: P.

4. Eds: E.

2. The code shall be unique for each activity carried out in the centre or equipment, in such a way that, with the corresponding letters and numbers, the activities carried out and the species are clearly identified. with which you work.

3. A Register of centres and equipment for the collection, storage or distribution of genetic material for animal reproduction for the national market or for the collection, storage or distribution of genetic material for the national market is established in the Ministry of the Environment, intra-Community trade, which shall be provided by data on approved centres or equipment communicated by the Autonomous Communities and acting on their respective registers, including the code covered by this Article.

4. The competent authorities shall notify any modification of such data of their records for updating in the central register.

Annually and before 31 March, those authorities shall submit a progress report which shall include a detailed list of approved centres or equipment and their genetic material, as at 31 December of the previous year.

5. This register includes those provided for in Article 5 of Royal Decree 2256/1994 of 25 November 1994 in Article 5 of Royal Decree 855/1992 of 10 July 1992 in Article 5 of Royal Decree 1148/1992 of 25 September 1992 and in the Article 11 of Royal Decree 1881/1994 of 16 September 1994.

Article 7. Sanctioning regime.

In case of non-compliance with the provisions of this royal decree, the regime of infringements and penalties provided for in Law 8/2003 of 24 April, or Royal Decree 1945/1983 of 22 June, for which they are regulated, will apply. infringements and penalties in respect of the defence of the consumer and of agri-food production, without prejudice to the civil, criminal or other responsibilities to which there should be. The other provisions on sanctioning in force approved by the Autonomous Communities shall apply.

Additional disposition first. Human and material resources.

The establishment and operation of the Register provided for in Article 6 shall be addressed with the personal and material resources available at the Ministry of the Environment, and the Rural and Marine Environment.

Additional provision second. Admission of genetic material from animals of endangered breeds and for scientific or experimental purposes.

Notwithstanding this royal decree, for genetic material coming from endangered listed breeds, or destined for scientific or experimental purposes, germplasm banks, or from animals of breeds of difficult handling (in the latter case, as regards the conditions of the extraction facilities, provided that it is carried out under equivalent conditions), the competent authority which officially recognised the organisation, organisations or associations or associations of breeders for the management of the Book the breed in question, on its own initiative or at the request of such associations or organisations, may authorise derogations from the requirements laid down in Article 3, provided that they do not pose a risk to public health or animal health. The competent authority shall inform the Commission of the derogations authorised to the Subdirectorate-General for the Conservation of Resources and Animal Nutrition of the Ministry of the Environment, and the Rural and Marine Environment, which shall communicate these derogations to the Commission. National Coordination for the Conservation, Improvement and Promotion of Livestock Races.

The exceptions that will be authorized will be communicated to the Ministry of the Environment, and the Rural and Marine Environment, which will give publicity to them through their website.

Additional provision third. Mutual recognition.

The requirements of this standard shall not apply to the genetic material of the legally collected, identified, stored, distributed and marketed bovine, ovine, caprine and porcine species and of the Equidae, in accordance with other specifications in the Member States of the European Union, or products originating in the EFTA countries Contracting Parties to the EEA Agreement or to States which have a Customs Association Agreement with the European Union.

First transient disposition. Coding of authorized centers and equipment.

The centres and equipment for the collection or storage of the genetic material already authorised and which have an authorisation code, will retain the same for that genetic material collected prior to the entry into force of the this rule. After this transitional period, the new code will be assigned to them, which they will use to replace the old one.

Second transient disposition. Identification of genetic material.

By way of derogation from the identification of the genetic material in Article 5, the material produced and identified before the entry into force of this standard shall retain the identification and may continue to use it until their stocks are exhausted.

Transitional provision third. Entry into force of Article 3.

A transitional period of 24 months is established from the entry into force of this royal decree for the enforcement of the health conditions described in points 1 (d) and 1 (e) of Article 3. necessary for national marketing for the reproductive purposes of semen, ova and embryos of ovine and caprine animals.

During the transitional period laid down in the preceding paragraph, semen, ova and embryos of animals of the ovine and caprine species which do not comply with the conditions laid down in Article 3 (1) (d) and (e) may not be marketed for reproductive purposes within the national scope. However, the competent authority of the autonomous community where it radiuses the livestock holding in which the animals are found to be able to authorise their placing on the market for reproductive purposes within the territorial scope of their autonomous community.

Transitional disposition fourth. Infrastructure of the centres and equipment.

Centers and equipment that are not authorized for intra-Community trade, prior to the entry into force of this standard, will have a period of 24 months from the entry into force of this royal decree, for adapt their infrastructure to the requirements laid down in Article 3.1. Such centres and equipment shall request a provisional authorisation from the competent authority of the autonomous community where they are located, and once obtained, they may only market genetic material on the national territory.

Single repeal provision. Regulatory repeal.

The following provisions are repealed:

(a) Decree 2499/1971 of 13 August on Regulatory Standards for Livestock Reproduction.

b) The Order of 29 January 1975, which regulates the participation of helpers for the application of artificial insemination.

(c) The Order of 31 October 1978 laying down specific rules on artificial insemination in pigs.

Final disposition first. Basic character and competence title.

This royal decree is of a basic nature, and is dictated by the provisions of Article 149.1, Rules 13 and 16 of the Constitution, which attribute exclusive competence to the State in the field of, respectively, bases and coordination of the overall planning of economic activity, and of general foundations and coordination of health.

Final disposition second. Ability to modify.

The Minister of the Environment, and the Rural and Marine Environment, is empowered to amend the Annexes in order to comply with Community or international regulations.

Final disposition third. Entry into force.

This royal decree will enter into force two months after its publication in the "Official Gazette of the State".

Given in Madrid, on June 17, 2011.

JOHN CARLOS R.

The Minister for the Environment, and the Rural and Marine Environment,

ROSA AGUILAR RIVERO

ANNEX I

Accompanying Document

Part A. Minimum document content for national trade in genetic material

1. Source:

a) Center or team identification code.

b) Source municipality.

c) Source Province.

2. Target:

a) The identification code of the target centre or holding.

b) Target municipality.

c) Target Province.

3. Transport temperature of the genetic material (environment, refrigeration or freezing).

4. Identification of genetic material.

a) Number of doses, eggs, or embryos.

b) Race, variety, or line.

c) System for the identification of the container and the genetic material.

5. Statement that the genetic material meets the requirements of this royal decree.

6. Place, date, signature and identification of the veterinarian of the centre or equipment, and seal of such centre or equipment.

Part B. Pure Races

Part B. 1 Data of the donor/fertilizer male (the latter in case of embryos)

1) Species (bovine, porcine, ovine and caprine) or Equidae.

2) Race and variety.

3) The issuing body and date of issue of the certificate.

4) Name and address of the Association of Breeders officially recognized for the management of the herd book, or the analogue register in case of imported doses.

5) Name and address of the breeder and owner.

6) Original number of enrollment in the genealogical book.

7) Date of birth.

8) Genotypes of genetic markers for the filiation test, if available.

9) Genealogy:

a) Parent (Original number of Enrollment in the Genealogical Book).

b) Mother (Original number of enrollment in the Genealogical Book).

c) Patric Grandfather (Original Number of Enrollment in the Genealogical Book).

d) Paterna Grandmother (Original Number of Enrollment in the Genealogical Book).

e) Maternal Grandfather (Original number of Enrollment in the Genealogical Book).

f) Maternal Grandmother (Original Number of Enrollment in the Genealogical Book).

10) All available results of the performance checks and the updated results of the genetic evaluation, with the name of the body that assessed the genetic value, relative to the animal itself and its parents and grandparents.

11) If available, the reliability of the genetic evaluation.

Part B. 2 Data of the female donor of embryos.

1) Species (bovine, porcine, ovine, caprine), or Equidae.

2) Race and variant.

3) The issuing body and date of issue of the certificate.

4) Name and address of the Association of Breeders officially recognized for the management of the herd book, or the analogue register in case of imported embryos.

5) Name and address of the breeder and owner.

6) Original registration number.

7) Date of birth.

8) Genetic markers for the lineage test, if available.

9) Genealogy.

a) Parent (Original number of Enrollment in the Genealogical Book).

b) Mother (Original number of enrollment in the Genealogical Book).

c) Patric Grandfather (Original Number of Enrollment in the Genealogical Book).

d) Paterna Grandmother (Original Number of Enrollment in the Genealogical Book).

e) Maternal Grandfather (Original number of Enrollment in the Genealogical Book).

f) Maternal Grandmother (Original Number of Enrollment in the Genealogical Book).

ANNEX II

Identifying Codes

Autonomous Community

Code
Andalusia	01
Aragon	02
Principality	03
Illes Balears	04
Canary	05
Cantabria	06
Castilla-La Mancha	07
Castilla y Leon	08
Catalonia	09
Extremadura	10
Galicia	11
Community	12
Region of Murcia	13
Navarra	14
Basque Country	15
The Rioja	16
Comunitat Valenciana	17
18
18
18
19

ANNEX III

BREED IDENTIFICATION CODES

Catalog Bovine Breeds Encoding

Race

BAV

Black Aviwood Iberian

BAM

BBN

Cachena

BCA

Minorquine

Fleckvieh

RW*

Code
Fomento Autoctonas
BAV
BAN
Lidia	BLI
Morucha	BMO
Pirenaica	BPI
Retint	BRT
Rubia Gallega	BRG
Autoctonas in danger extinction
Albera	BAB
BAS
BAM	BAM
Black-wood (var. White-horn)	BANB
Berrenda in Colorado	BBC
Berring	BBZ
Betizu	BBZ
BBZ
Bruna	BBP
BCH
	Caldela
BCN
Frieiresa	BFR
Limia	BLM
	Mallorcan			Marismena
BMR
		BMN
Monchina		BMC
Morucha (Black Var)	BMON
Murciana-Uprising	BMU
Black Andalusia	BNA
Pajuna	BPJ
Palmera	BPM
Passive	BPS
Sayaguesa	BSY
Serrana	BSN
Serrana de Teruel	BST
Terrain	BTN
Tudanca	BTU
Vianese	BVN
Races in Spain
	BD*
CH*
SM*
HO*
Limo	LM*
	BS*
Montana	BSM
RW*
RW*

* ICAR encoding.

Catalog Ovines Races Encoding

Race

OCA

Ibicenca

Mallorcan

OMAN

ORM

ORM

Races of the European Union

Code
Fomento Autoctonas
Castellana	OCS
Churra		Lacha
Lacha
Manchega		WCO
Merin	OME
Navarra		ONA
Teruel Ojinegra		Rasa Aragonesa
ORA
	OSE
extinction hazard autoctonas
OAL
OAL
	OAN
OAR	OAR
	OAR
	OAR
	Canary	OCN
	OCN	OCP
Black Variety Carranzana	OCAN
	OCR
Variety	OCSN
Chamarita	CMO
Churra Lebrijana	Churra Tensin
	Churra Tensina		Colmensand
OCL
Gallega			Guirra
OGI
Ibicenca		OIB
Lojena			Maellana
OML
		OMQ
OMAN
	Minorquine	OMN
Merine Variety Black	OMEN
Grazalema Merine	OMG
OMT
OJL	OJL		OJL
OPL
OPL
	ORP
	ORM
Roya Bilbilitana
Molar Rubia	ORU
Sasi Ardi	OSR
Talaveran	OTV
Xalda	OXL
Xtab	OXQ
Races in Spain
Berrichon du Cher	OBE
Charmoise	OCI
Fleischschaf	Ile de
	OIF
Landschaff	Ile OLN
Premature Merino	OMP
	Lacaune	OLC
country Races
Assaf	OAF
Races Spanish
Salz	OSZ

Catalog Goat Races

Race

Tinerfena

Code
Fomento Autoctonas
Majorera	CMJ
	Malaguena	CMA
Murciana-Granadin	Palmera
CPA
of the Tabs	CAM
CAG
CBA	CBA
CBA
Celtiberic White	CBC
Bermella	CBE
Of The Guadarrama	CGU
Florida	CFL
Gallega	CGA
Ibicenca	CIB
Jurdana	CJU
Mallorcan	CML
Moncaine
Black Serrana	CNS
Payoya	CPY
Pirenaica	CPI
Retint	CRE
Verata	CVE
Races of the European Union

Catalog Porcine Races Catalog

Race

Landrace

Code
Fomento Autoctonas
Iberico	GDP
Iberian Variety Retinto	PIBR
Variety Entrepreneur	PIE
Extinction Autoctonas
Celta	PCL
Chato Murciano	PCH
Euskal Txerria	PET
PGA
Variety Torbiscal	PIBT	PIBT
Iberian Lampino Variety	PIBL
Iberian Jabugo Spotted Variety	PIBM
Black Canary	PNC
Black Mallorcan	PNM
Races in Spain
White Belga	PBB
PDC
PDC
	Hampshire	PHA
PLD
PLW
PLW
PPT
PPT

Catalog Equine Races

Race

EJN

EAA

EPS

EPS

Code
Fomento Autoctonas
Spanish	EES
extinction hazard Autoctonas
Asturcon	EAS
Burguete	EBU
Mount the Basque Country	EMP
Gallega Race Horse
Hispanic-Arabic	EHA
EHB
	EHB
EJN
Losina	ELO
Mallorcan	EMA
Marismena	EMR
EME	EMO
EMO
EMO
EMO
Integrated Races in Spain
	EAR
EAA
Spanish Trotter	ETR
Other registered equidae
Sport Horse	ECD

Catalog Asnal Races Encoding

	Code
Extinction Autoctonas
Andaluza	EAN
Asno Incartations	EAE
Balear
Catalan	ECT
Majorera	EMJ
Zamorano-Lions	EZL

ANNEX IV

Minimum health conditions for semen, ova and embryos

1. Sanitary conditions applicable to semen of animals of the porcine species.

a) Conditions for the authorization of collection centers.

The conditions for the approval of collection centres are those laid down in Annex A to Commission Decision 1999 /608/EC of 10 September amending the Annexes to Council Directive 90 /429/EEC on the laying down the animal health rules applicable to intra-Community trade in and imports of semen of animals of the porcine species.

(b) Health conditions for animals of the porcine species.

The health conditions for domestic animals of the porcine species are those laid down in Annex B to Commission Decision 1999 /608/EC of 10 September 1999 and Decision 2000 /39/EC of the European Parliament and of the Council of 10 September 1999 on Commission of 16 December 1999 amending Annex B to Council Directive 90 /429/EEC laying down the animal health rules applicable to intra-Community trade in and imports of semen of animals of the European Union Porcine species.

c) Conditions for the collection, treatment, storage and transport of semen.

The conditions for the collection, treatment, storage and transport of semen are those laid down in Annexes A and C to Commission Decision 1999 /608/EC of 10 September.

2. Sanitary conditions applicable to semen of animals of the ovine and caprine species, or Equidae.

(a) Conditions for the approval of collection centres. The conditions for the approval of the collection centres are those laid down in the Annex to Commission Regulation (EU) No 176/2010 of 2 March 2010 amending Annex D to Council Directive 92/65/EEC as regards: semen collection and storage centres, embryo collection and production equipment and the conditions applicable to donor animals of the equine, ovine and caprine species and the handling of semen, ova and embryos of the semen same.

(b) Health conditions for animals of the ovine and caprine species or Equidae. The health conditions required are those laid down in the Annex to Commission Regulation (EU) No 176/2010 of 2 March 2010.

c) Conditions for the collection, treatment, storage and transport of semen. The conditions for the collection, treatment, storage and transport of semen are laid down in the Annex to Commission Regulation (EU) No 176/2010 of 2 March 2010.

3. Health conditions applicable to ova and embryos of animals of the ovine, caprine and porcine species or Equidae.

(a) Conditions applicable to donor females.

1. Only donor females which, to the satisfaction of the official veterinarian or, where appropriate by the approved or authorised veterinarian, satisfy the requirements of the legislation may be used for the collection of embryos or ova. relevant for intra-Community trade in live animals for breeding and for the species in question and originating from holdings which also comply with them.

2. In addition to the requirements of Royal Decree 1716/2000 of 13 October on sanitary rules for the intra-Community trade in bovine animals and swine, female donors of the porcine species must comply with the Aujeszky's disease requirements set out in Royal Decree 360/2009 of 23 March 2009 laying down the basis for the coordinated programme for the control, control and eradication of Aujeszky's disease, except in the case of in vivo obtained embryos treated with trypsin.

3. The provisions of Royal Decree 1941/2004 of 27 September 2004 will apply to female donors of the ovine and caprine species.

4. In addition to the requirements laid down in Royal Decree 1347/1992 of 6 November 1992 amending the rules for the control of African horse sickness and laying down the animal health conditions governing movements Intra-Community trade in equidae and imports of such animals from third countries, donor mares:

-Not to be used for natural reproduction for at least 30 days prior to the date of collection of the ova or embryos, or between the day of the first sample taken to carry out the tests referred to continuation and the day of collection of the ova and embryos;

-To be tested negative in the agar gel immunodiffusion test (Coggins test) or ELISA for the detection of equine infectious anaemia performed with blood samples taken initially in the 30 days prior to the date of the test. of the first collection of ova or embryos and subsequently every 90 days during the collection period;

-Must be tested for contagious equine metritis by isolation of Taylorella equigenitalis performed with samples taken from the mucous surfaces of the pit and the breast of the clitoris in two consecutive, and with another crop sample taken from the endometrial cervix during one of the patients, with negative results in all cases after a 7-to 14-day culture.

(b) Conditions applicable to the authorisation of the embryo production centres.

The conditions for the authorisation of the embryo production centres are those set out in the Annex to Commission Regulation (EU) No 176/2010 of 2 March 2010.

c) Conditions applicable to collection, processing, storage, storage.

The conditions for collection, treatment, storage, storage are those laid down in Chapter III of the Annex to Commission Regulation (EU) No 176/2010 of 2 March 2010.

(d) Conditions applicable to semen of animals of the porcine species used for the insemination of donor females.

The conditions applicable to the semen of animals of the porcine species used for the insemination of the donor females are those laid down in Annex B to Commission Decision 1999 /608/EC of 10 September 2000 and the Commission Decision 2000 /39/EC of 16 December amending Annex B to Council Directive 90 /429/EEC.