The import of pathogens and pathogenic agents is only permitted under a licence issued under The Importation of Pathogenic Agents Order, 1997 (S.I. No. 373 of 1997).
Pathogens that do not comply with import conditions and controls can be seized either for destruction or return to the country of origin at the importers expense.
The import licence referred to below is issued without prejudice to import controls in place for other than for public or animal health reasons and does not exempt importers from any prohibition, regulation or restriction imposed by any other agency or department.
What you must do
Fill in the attached form and return it to the address below.
When importing, there are certain rules and regulations you must obey:
consignments must be transported with appropriate UN approved packaging and compliant with TATA and ADR Regulations
each consignment must be accompanied by a copy of the VET 40 licence and documents providing the name and address of consignor and consignee, destination laboratory, type of product and quantity
the exterior of each vial, bottle or tube must be disinfected prior to packaging for dispatch
the container(s) must be clearly labelled with the type of product and quantity and contain the import licence number and the consignee and destination laboratory's name and address
the importer is responsible for ensuring that the person(s) consigning and dispatching the material to Ireland is/are aware of and comply with the undertakings in the application for this licence and the conditions contained in this licence
when importing a pathogen from a third country, the consignment must be presented for inspection to an EU approved Border Control Post (BCP) listed on this page.
Shannon Airport is currently the only EU approved BIP in Ireland for such consignments
the importer or agent of the importer must provide a minimum of 24 hours advance notification of arrival on EU territory to the approved BIP through which it is proposed to import the consignment (i.e. Shannon Airport). This done by submitting Part 1 of the Common Health Entry Document (CHED) – ref. Annex III to Regulation (EC) No. 136/2004
from the point of entry into Ireland, the consignment must remain in its original packaging and be transported directly to the laboratory of use without coming into contact with any animals
the product and any product derived from it are for use at the laboratory at point (6) for the purposes stated in the application and must not to be sold, supplied or dispatched from that laboratory
as a minimum the containment measures specified for containment level 2' must be implemented in the laboratory at all times
any potentially infectious liquid waste must be disinfected in excess sodium hypochlorite (or suitable alternative effective disinfectant) prior to disposal via the drain. The procedure must be defined in an SOP and volumes noted in a worksheet
all potentially dirty drains will have p traps of suitable depth and will be flushed at regular intervals to prevent drying out. This must be defined in an SOP
any substantive variation from the information provided in the licence application should be notified to DAFM and a reapplication may be sought if appropriate
any inspection report by a state or international agency containing a negative finding shall be notified to DAFM without delay
if potential animal health risks, other than those already identified in your application arise work should be suspended and DAFM notified immediately
disposal of all waste material must be as stated in the licence application
this licence is granted under the Importation of Pathogenic Agents Order, 1997 and nothing in this licence gives exemption from any prohibition or restriction imposed by any other legislation
records relating to the product imported under this licence containing an inventory of stock and date acquired and forming a complete audit trail from the time of importation shall be maintained for at least three years and be made available for inspection by an officer of this department on request
the importer or his agent shall provide all necessary assistance to an officer to enable him/her to inspect the products and records
an inventoried facility pathogen archive must be maintained by the laboratory and be made available upon request to an officer
where relevant, any licence required from the Environmental Protection Agency for genetically modified organisms must be in place before importation takes place
To expedite the processing of an application form for a VET 40 pathogen licence, the applicant may email a scanned copy of the signed application form and a copy of the Certificate of Registration to AnimalProductImports@agriculture.gov.ie
However, the licence will not be issued until the original signed copy of the application form has been received.