English

Cuardaigh ar fad gov.ie

Foilsiú

Ovine and Caprine Semen, Ova and Embryos



General Principles and Relevant Legislation

‘Germinal products’ means semen, oocytes and embryos intended for artificial reproduction.

1. The requirements for entry into the Union of germinal products are based on the requirements for entry into the Union of live animals. The list of countries, territories or parts thereof authorised for the export of ovine and caprine germinal products are laid down in Annex X of Regulation (EU) 2021/404.

2.Regulation (EU) 2016/429 (‘Animal Health Law’) and Commission Delegated Regulation (EU) 2020/692 lay down the rules for the entry into the Union of germinal products.

3.Commission Delegated Regulation (EU) 2020/692, Articles 91 and 92 describes the rules for entry into the Union, and the movement and handling after entry of consignments of ovine and caprine germinal products.


Import Conditions

Chapter 1 of Part V of the Animal Health Law sets out the requirements for entry into the union of germinal products of ungulates as follows;

(a) they must come from a listed third country or territory listed in Annex X of Regulation 2021/404

(b) they must come from establishments which are approved and listed - Establishment Lists - TRACES NT (europa.eu)

(c) they must fulfil the necessary animal health requirements for entry into the Union;

(d) they must be accompanied by an animal health certificate and by declarations and other documents where required.

- Title 1 of Part III of Commission Delegated Regulation (EU) 2020/692 (Articles 79-85a) sets out the specific animal health requirements for germinal products of ungulates. The donor ovine and caprine animals must have been resident in the third country for six months prior to the date of collection and comply with the other residency requirements in Article 80(b) of Reg 2020/692.

- Individually identified as per Article 21 of Reg 2020/692

- From approved and listed establishments as per Establishment Lists - TRACES NT (europa.eu)

- The germinal products must be marked, packaged, and transported in accordance with Articles 83 and 84.

Chapter 4 of Title I of Part III sets out specific animal health requirements for ovine and caprine germinal products, regarding the establishment of origin’s freedom from infection with Brucella abortus, B. melitensis and B. suis.


Veterinary Certification

1. Consignments of ovine and caprine germinal products from third countries must be accompanied by a health certificate, which conforms to the model as laid down in Commission Implementing Regulation 2021/403, which is signed by an official veterinarian or inspector of the veterinary authority in the country of origin.

Article 21 of this Regulation describes the model certificates available, the models of which are in Annex II of the same Regulation.

The model certificate type depends on when the germinal products were collected and produced, and the type of establishment from which it was dispatched.

The animal health certificates to be used for the entry into the Union of certain types of germinal products of ovine and caprine animals shall correspond to one of the following models.

OV/CAP-SEM-A-ENTRY (chapter 48)

OV/CAP-SEM-A-ENTRY
Amharc amharc

OV/CAP-SEM-B-ENTRY (chapter 49)

OV/CAP-SEM-B-ENTRY
Amharc amharc

OV/CAP-OOCYTES-EMB-A-ENTRY (chapter 50)

OV/CAP- OOCYTES-EMB-A-ENTRY
Amharc amharc

OV/CAP-OOCYTES-EMB-B-ENTRY (chapter 51)

OV/CAP-OOCYTES-EMB-B-ENTRY
Amharc amharc

OV/CAP-GP-PROCESSING-ENTRY (chapter 52)

OV/CAP-PROCESSING-ENTRY
Amharc amharc

OV/CAP-GP-STORAGE-ENTRY (chapter 53)

OV/CAP-GP-STORAGE-ENTRY
Amharc amharc

Document Submission

1. Consignments of germinal products entering the EU must be inspected at an EU-approved Border Control Post (BCP) where Member States' official veterinarians ensure they fulfil all the requirements provided for in EU legislation.

2. The person responsible for the load being imported (the importer or a customs agent acting on their behalf) must give the BCP at the intended point of entry advance notification of the arrival of the consignment.

There is a required minimum pre-notification notice period of at least 24 hours’ notice in advance of the consignment’s arrival.

Failure to submit correct documentation within this timeline may result in significant delays in the consignment being processed through the Border Control Post.

Pre-notification is given by the submission of Part 1 of the Common Health Entry Document (CHED-P), as is laid down in Commission Implementing Regulation (EC) No. 2019/1715, through the online TRACES system.

3. Copies of other supporting documentation associated with the consignment should be submitted at this time as well - such as the Health Certificate, Invoice, Packing list and so on.

4. Necessary documents and logistical information must be submitted 24 hours in advance via the DAFM Import Portal


Border Control

1. All germinal products from third countries require veterinary checks at their point of entry into the European Union, as listed in the Annex to Commission Implementing Regulation (EU) 2021/632.

2. EU harmonised import controls are carried out at an approved Border Control Post (BCP) that is designated to deal with that type of import. A consignment of ovine or caprine germinal products may only enter Ireland through an approved Border Control Post (BCP) designated ‘POA’ (products of animal origin).

Dublin Port, Dublin airport, Shannon airport and Rosslare port BCPs are all approved for ‘POA’.

3. Providing all the documentation has been submitted correctly and within the correct timeframes, a large proportion of the documentary check can be commenced in advance of the consignment’s arrival. This includes examination of the veterinary certificate and other documents accompanying a consignment.

The original hard copy of the health certificate must travel with the consignment and will be checked and held at the BCP at the point of entry into the EU.

4. Provided all is in order with the documentary check, the consignment of ovine or caprine germinal products will then be subject to an identity check and physical check with/without sampling as appropriate at the BCP.

5. Upon satisfactory completion of the required checks, the decision is entered in Part 2 of the CHED which must accompany the consignment to the first place of destination referred to in the CHED.

6. If the consignment does not meet the import requirements, the consignment may be rejected entry and re-exported or destroyed if necessary.