Summary

Amends the

in relation to: the supply of medical devices that are not on the Therapeutic Goods Register; the listing of export-only variations of certain medicines already on the register; permissible ingredients for inclusion in medicines; information that may be considered by the minister when reviewing initial decisions; the process for submission and approval of product information for medicines; the power of the secretary to make declarations that goods are therapeutic goods; the revised business processes which apply to prescription medicines; and the secretary’s information gathering powers.