Food and Drug Regulations

G.02.003.2 Subject to section G.02.003.3, the Minister shall, after examining the information and documents required under sections G.02.003 and G.02.003.1, issue a dealer’s licence that contains

• (a) the licence number;

• (b) the name of the applicant or the title of the position they hold, as the case may be, or, if the applicant is a corporation, its corporate name;

• (c) a list of the activities that are permitted;

• (d) the address of the premises at which the licensed dealer may carry on the permitted activities;

• (e) the name of the controlled drug for which the activities are permitted;

• (f) the security level at the premises;

• (g) the effective date of the licence;

• (h) the expiry date of the licence, which may not be later than three years after its effective date;

• (i) any conditions to be met by the holder of the licence to

  • (i) ensure that an international obligation is respected,

  • (ii) provide the security level referred to in paragraph (f), or

  • (iii) reduce the potential security, public health or safety hazard, including the risk of the controlled drug being diverted to an illicit market or use;

• (j) in the case of a producer of a controlled drug, the quantity of the controlled drug that may be produced under the licence and the period during which that quantity may be produced; and

• (k) in the case of the maker or assembler of a product or compound that contains a controlled drug but is not a test kit, an annexed list that sets out the following information for each type of product or compound that may be made or assembled under the licence:

  • (i) the licence number,

  • (ii) the brand name, if any, of each product or compound,

  • (iii) the controlled drug in each product or compound,

  • (iv) the strength per unit of the controlled drug in each product or compound, and

  • (v) the quantity or package sizes of each product or compound.