consider and approve applications for licence to manufacture pharmaceutical products, subject to any conditions it thinks fit to impose;
(b)
revoke a licence to manufacture pharmaceutical products, suspend a licence to manufacture pharmaceutical products for a specified period, issue warning letter(s) to the licensed manufacturer or vary a condition of the licence to manufacture pharmaceutical products in the circumstances specified in Regulation 29 of the Pharmacy and Poisons Regulations;
(c)
consider and approve applications for registration as authorized person or renewal of registration as authorized person, subject to any conditions it thinks fit to impose; and
(d)
cancel the registration as authorized person, suspend the registration as authorized person for a specified period, issue warning letter(s) to the registered authorized person or vary a condition of the registration as authorized person in the circumstances specified in Regulation 30F of the Pharmacy and Poisons Regulations.