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CIVIL AVIATION SAFETY REGULATIONS 1998 - REG 99.210 Notices of Sample A results

CIVIL AVIATION SAFETY REGULATIONS 1998 - REG 99.210

Notices of Sample A results

Laboratory to CASA

  (1)   As soon as practicable after a confirmatory test is conducted on Sample A of a body sample by an approved laboratory, the laboratory must send to CASA a dated, written notice that includes the following:

  (a)   the date and time of receipt of the body sample at the laboratory;

  (b)   the sample identifier for the body sample;

  (c)   a statement as to whether the tamper - evident seals on the specimen tubes containing the body sample were intact on receipt by the laboratory;

  (d)   the list of testable drugs that the approved tester of the initial drug test asked to be tested;

  (e)   the date and time that Sample A was tested;

  (f)   the method used for the testing;

  (g)   the target concentrations of the testing;

  (h)   the result of the test;

  (i)   a statement about whether the body sample has been tested in accordance with these Regulations, and any conditions attached to the laboratory's National Association of Testing Authorities accreditation;

  (j)   the name of the person who declared the results of the test.

  (2)   The notice must be signed by the laboratory's approved person.

CASA to donor--oral notice

  (3)   As soon as practicable after CASA receives the notice from the laboratory, CASA must give oral notice to the donor of the body sample of the confirmatory test result on Sample A.

CASA to donor--written notice

  (4)   As soon as practicable after CASA gives the oral notice, CASA must give a written notice to the donor that includes the following:

  (a)   the sample identifier for Sample A and Sample B;

  (b)   the list of testable drugs that were tested for;

  (c)   a statement as to whether the tamper - evident seals on the specimen tubes containing the body sample were intact on receipt by the approved laboratory that tested them;

  (d)   the date and time that Sample A was tested;

  (e)   the method used for the testing;

  (f)   the target concentrations of the testing;

  (g)   the result of the test;

  (h)   a statement about whether the body sample has been tested in accordance with these Regulations and any conditions attached to the laboratory's National Association of Testing Authorities accreditation;

  (i)   if the result of the test is a positive result:

  (i)   information about the donor's rights to have Sample B tested; and

  (ii)   information about how the donor gets Sample B tested and the costs associated with that testing.

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