Food and Drug Regulations

Marginal note:Declaration

G.02.046 The holder of an export permit must provide the Minister, within 15 days after the day of export of the controlled drug specified in the permit, with a declaration that contains the following information:

• (a) their name and the numbers of their dealer’s licence and the export permit that applies to the controlled drug;

• (b) with respect to the controlled drug,

  • (i) its name, as specified in the dealer’s licence,

  • (ii) if it is a salt, the name of the salt, and

  • (iii) its quantity;

• (c) if the controlled drug is contained in a product that they have exported,

  • (i) the brand name of the product,

  • (ii) the drug identification number that has been assigned to the product under section C.01.014.2, if any, and

  • (iii) the strength per unit of the controlled drug in the product, the number of units per package and the number of packages; and

• (d) the name of the customs office from which the controlled drug was exported and the date of export.