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- Point in Time (06/04/2009)
- Original (As adopted by EU)
Commission Regulation (EC) No 318/2007 of 23 March 2007 laying down animal health conditions for imports of certain birds into the Community and the quarantine conditions thereof (Text with EEA relevance) (repealed)
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There are currently no known outstanding effects for the Commission Regulation (EC) No 318/2007 (repealed), ANNEX IV.
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Approved quarantine facilities and centres shall comply with the conditions set out in Chapters 1 and 2.
have an efficient control system so as to ensure adequate surveillance of the animals;
be under the control and responsibility of the official veterinarian;
be cleaned and disinfected in accordance with a programme approved by the competent authority after which there shall be an appropriate resting period; the disinfectants used must be approved for that purpose by the competent authority.
the approved quarantine facility or unit of an approved quarantine centre must be cleaned and disinfected and then be kept free of birds for at least seven days before the imported birds are introduced;
the consignment of birds must come from a single approved breeding establishment in the third country of origin and be introduced over a period of not more than 48 hours;
the quarantine period must start when the last bird is introduced;
the approved quarantine facility or unit of an approved quarantine centre must be emptied of birds, cleaned and disinfected at the end of the quarantine period.
the date, number and species of birds entering and leaving for each consignment;
copies of the animal health certificates and the Common Veterinary Entry Documents accompanying the imported birds;
individual identification numbers of the imported birds, and in case of identification by microchip the details of the type of microchip and the reader used shall be recorded;
if in the quarantine facility or centre sentinal birds are used, the number and placing of the sentinel birds in the quarantine facility or centre;
any significant observation: cases of illness and number of deaths on a daily basis;
dates and results of testing;
types and dates of treatment;
persons entering and leaving the quarantine facility or centre.
The procedures for partly or completely suspending, withdrawing or re-granting approval of quarantine facilities and centres shall comply with the conditions set out in this Chapter:
Where the competent authority finds that a quarantine facility or centre no longer complies with the conditions set out in Chapters 1 and 2, or there has been a change of use which is no longer covered by Articles 3(e) and (f), it shall inform the Commission of this fact. Such quarantine facilities or centres shall not be used for imports in accordance with this act.
Approval shall only be re-granted to a quarantine facility or centre when the conditions laid down in Chapters 1 and 2 are again fulfilled.
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