(a) Define “pharmaceutical product” and “advanced therapy product” under the Pharmacy and Poisons Ordinance. 

(b) Describe the labelling requirements for a pharmaceutical product to be supplied in Hong Kong as stipulated under the Pharmacy and Poisons Ordinance and its Regulations. 

(c) What additional labelling requirements will apply if the medicine (i) is a lotion; (ii) is for the treatment of an animal; (iii) contains a Part 1 Poison (except Schedule 3 Poison); and (iv) contains a Schedule 3 poison?

(20 marks) 

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