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3. An assessment carried out for the purposes of regulation 7 shall include—
(a)identification of the harmful properties of the recipient and, where appropriate, the donor organism;
(b)identification of any harmful properties associated with the vector or inserted material, including any alteration in the existing properties of the recipient;
(c)identification of the provisional level of risk associated with the genetically modified organisms;
(d)selection of containment and other protective measures on the basis of—
(i)the provisional level of risk, and
(ii)the characteristics of the activity involving genetic modification;
(e)adjustment of the level of risk in the light of the matters referred to in sub-paragraph (d) above; and
(f)review and reconsideration of the containment and other protective measures in the light of the steps required by sub-paragraphs (a) to (e) above.
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