Importing country requirements
It is the exporter's responsibility to ensure that the animal meets the importing country requirements.
- Where an importing country issues an import permit, the exporter must ensure the animal meets any requirements in the permit.
- Australia is free of:
- Bovine tuberculosis
- Contagious Bovine Pleuropneumonia (CBPP)
- Contagious Nodular Dermatosis (Lumpy Skin Disease)
- Foot and Mouth Disease
- Pest des petits ruminants (PPR)
- Rift Valley Fever
- No cases of disease caused by Schmallenberg virus have been detected or reported in Australia.
- The in vivo embryo collection (EC) equipment, the in vitro embryo production (EP) and the fixed or mobile embryo manipulation laboratory (LM) are approved and supervised by the Veterinary Authority of the exporting country.
- The LM shall not be located and the EC or EP did not act in areas with sanitary restrictions related to the diseases of bovine and bubaline, whose transmission may occur through the embryos.
- The donors remained in the herd of origin for a minimum period of thirty (30) days prior to the collection of the embryos. In that period, as well as, in the thirty (30) days post collection, no case of Bovine Viral Diarrhea was officially reported in that herd and the referred donors did not present any clinical sign of diseases that could be transmitted by embryos.
5.1. In the case of embryos produced in vitro: the donor animals do not come from establishments that are subject to restrictions in relation to foot-and-mouth disease (FMD) or peste des petits ruminants (PPR), and no tissue was extracted and no oocytes were aspirated in an infected area or that are subject to infection or veterinary restrictions in relation to the aforementioned diseases. (strike through if not applicable).
- The semen used for the production of the embryos to be exported was obtained in a Semen Collection and Processing Center (CCPS) approved by the Veterinary Authority of the country of origin of the semen, complying with the "General hygiene conditions in the semen collection and treatment centers ", and those described in the Chapter referred to "Semen collection and treatment of bovines, small ruminants and male pigs "of the OIE Terrestrial Code.
- The embryos were collected, processed and stored in accordance with the recommendations established in the OIE Terrestrial Code and in the Manual of the International Embryo Transfer Society (IETS). In all cases, the protocol which includes the additional sluices with trypsin, contemplated in said Manual, was used.
7.1. After sluicing, the pellucid zone of each embryo had been examined on its surface, using a microscope with an increase of no less than 50X, being intact and free of adherent material.
- All equipment used to collect, produce, handle, sluice, freeze and store the embryos was sterilized before usage, in accordance with the recommendations of the IETS Manual.
- All biological products of animal origin used in the collection, production, processing and storage of embryos are free of microorganisms. Fetal bovine serum, serum albumin or any other product of ruminant origin used come only from countries recognized by the OIE as negligible risk or controlled risk and without any case registration, in relation to Bovine Spongiform Encephalopathy.
- The embryos were stored in new containers washed and disinfected, using liquid nitrogen of first-use, for a minimum period of thirty (30) days prior to shipment. During that period, no clinical signs of infectious diseases were recorded, in the establishment where the embryos were collected and in the female donors.
Method of disinfection and active ingredient:
Date of disinfection:
- At the time of shipment, the container was sealed under the supervision of the Veterinary Authority of the exporting country and the seal number is registered in the Official Health Certificate.
Number of the seal(s) on the container (s)………………………
In addition to the health certificate, the export must be accompanied by a declaration from the LM’s veterinary officer (an ECT-EPT certificate) in the following form:
Basis for Micor entry
Health certificate agreed 30 May 2019
Entry last reviewed 12 March 2020