A certificate under section 57(4A) of the Act must contain the following particulars—
(a) a statement by the approved analyst that he or she is an approved analyst within the meaning of section 57 of the Act; and
(b) a statement as to the method of analysis used; and
(c) a statement that a substance that is, or is capable of being, a drug for the purposes of the Act was present in the sample of blood analysed; and
(d) the name of the substance found to be present in the sample of blood analysed; and
(e) the name and signature of the approved analyst; and
(f) the date on which the analysis was conducted; and
(g) a description of the contents of the identification label referred to in regulation 11(1)(d) attached to the container in which the blood sample is placed.