(1) A local representative for a regulated product shall be appointed by the relevant body.

(2) The local representative

(a) shall monitor the safety of the product granted marketing approval, and

(b) shall report an adverse effect or event to the Authority during the period under which the product is registered.

(3) The Authority shall continually monitor the safety of the products regulated under this Act by analysis of the adverse effect or event reports and by any other means and take appropriate regulatory action when necessary.