I think what we preliminarily read into part (ii) of (c) is a sort of form of self-attestation. The current human pathogen importation regulation actually sets out in some detail specific requirements in terms of information provided, which is not detailed in this particular section. Also, it will not allow for a specific objective look at whether someone is following the laboratory biosafety guidelines and is relying solely on self-attestation.
On March 31st, 2009. See this statement in context.