A certificate under section 86I(7) of the Act must contain the following particulars—
(a) a statement by the approved analyst that the analyst is an approved analyst within the meaning of section 86I(1) of the Act;
(b) a statement as to the method of analysis used;
(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;
(d) the name of the substance found to be present in the sample of blood analysed;
(e) the name and signature of the approved analyst;
(f) the date on which the analysis was conducted;
(g) a description of the identification label referred to in regulation 8(1)(d) attached to the container in which the blood sample is placed.