South Australian Current Regulations

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LIVESTOCK REGULATIONS 2013 - REG 23

23—Conditions of registration

Registration under section 20 of the Act of a veterinary diagnostic laboratory is subject to the following conditions:

            (a)         the laboratory must be supervised by a person or persons approved by the Chief Inspector;

In respect of the supervision of animal disease diagnosis carried out at the laboratory, the person must be a veterinary surgeon.
In respect of the supervision of residue analysis carried out at the laboratory, the person must hold appropriate qualifications.

            (b)         the methods used at the laboratory for animal disease diagnosis must conform to the Australian Standard Techniques for Animal Diseases published for the Australian Agricultural Council (Standing Committee on Agriculture) by CSIRO Australia, as in force from time to time;

            (c)         if a result from any test or analysis carried out at the laboratory indicates that any livestock or livestock product or other property is, or is likely to be, affected with a notifiable condition the result must be reported to the Chief Inspector by the quickest practicable means, together with such further information as the Chief Inspector may reasonably require;

            (d)         records of results from each test or analysis carried out at the laboratory must be kept for a period of at least 7 years;

            (e)         a laboratory sample or specimen affected or reasonably suspected of being affected with a notifiable condition must not, without the approval of the Chief Inspector—

                  (i)         be brought into the laboratory from interstate or overseas; or

                  (ii)         be sent from the laboratory out of the State;

            (f)         laboratory samples or specimens or records of results from a test or analysis carried out at the laboratory, must, at the request of the Chief Inspector, be provided to the Chief Inspector or a person nominated by the Chief;

            (g)         the laboratory must participate in a quality assurance program approved by the Chief Inspector.



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