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Cannabis Regulations (SOR/2018-144)

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Regulations are current to 2019-06-20 and last amended on 2019-01-15. Previous Versions

PART 2Licensing (continued)

Processing Licences (continued)

Marginal note:Minister’s approval

  •  (1) A holder of a licence for processing must obtain the Minister’s approval before

    • (a) designating or replacing an alternate quality assurance person; and

    • (b) replacing the quality assurance person by an individual, other than by the alternate quality assurance person.

  • Marginal note:Application — content

    (2) The holder of a licence for processing must, for the purpose of obtaining the Minister’s approval, submit an application that includes the following:

    • (a) the name and date of birth of the proposed alternate quality assurance person or the proposed quality assurance person;

    • (b) a description of the proposed quality assurance person’s or the proposed alternate quality assurance person’s qualifications in respect of the matters referred to in subsection 19(1); and

    • (c) a declaration, signed and dated by the responsible person referred to in section 37, indicating that all information provided in support of the application is correct and complete to the best of their knowledge.

  • Marginal note:Additional information

    (3) The Minister may, on receiving an application for approval, require the submission of any additional information that pertains to the information contained in the application and that is necessary for the Minister to consider the application.

Marginal note:Micro-processing — threshold

  •  (1) A holder of a licence for micro-processing must not possess, in a calendar year, cannabis of one or more classes of cannabis — other than cannabis plants and cannabis plant seeds — that has been sold or distributed to them the total amount of which, as determined in accordance with the table to this section, is equivalent to more than 600 kg of dried cannabis.

  • Marginal note:Equivalency

    (2) The cannabis referred to in subsection (1) is exempt from the application of subsection 2(4) of the Act and a quantity referred to in column 2 of the table to this section in respect of any class of cannabis referred to in column 1 is deemed to be equivalent to 1 kg of dried cannabis.

  • Marginal note:Non-application

    (3) Subsection (1) does not apply if the holder also holds a licence for micro-cultivation in relation to the same site and the cannabis that is sold or distributed to them is exclusively from that site.

    TABLE

    Column 1Column 2
    ItemClass of cannabisAmount that is equivalent to 1 kg of dried cannabis
    1dried cannabis1 kg
    2fresh cannabis5 kg
    3solids containing cannabis10 kg
    4non-solids containing cannabis10 kg
    5cannabis solid concentrates0.25 kg
    6cannabis non-solid concentrates0.25 kg

Licence for Analytical Testing

Marginal note:Authorized activities

  •  (1) Subject to the other provisions of these Regulations, a holder of a licence for analytical testing is authorized, for the purpose of testing, to conduct those of the following activities that are authorized by the licence:

    • (a) to possess cannabis; and

    • (b) to obtain cannabis by altering its chemical or physical properties by any means.

  • Marginal note:Offer

    (2) A holder of a licence for analytical testing that is authorized to conduct the activity referred to in paragraph (1)(b) is also authorized to offer to conduct that activity.

  • Marginal note:Use of organic solvent

    (3) A holder of a licence for analytical testing that is authorized to conduct the activity referred to in paragraph (1)(b) is also authorized to alter or offer to alter the chemical or physical properties of cannabis by the use of an organic solvent when conducting that activity.

Marginal note:Head of laboratory

  •  (1) A holder of a licence for analytical testing must retain the services of one individual as the head of laboratory who must work at the site set out in the licence and who is responsible for the testing referred to in section 91.

  • Marginal note:Qualifications

    (2) The head of laboratory must have sufficient knowledge of the provisions of the Act and these Regulations that apply to the holder of the licence for analytical testing, have knowledge and experience related to the duties of the position and possess a degree in a science related to the work to be carried out that is awarded by a Canadian university or, if awarded by a foreign university, that is recognized by a Canadian university or a Canadian professional association.

  • Marginal note:Alternate

    (3) A holder of a licence for analytical testing may designate one or more individuals as the alternate heads of laboratory who are qualified to replace the head of laboratory.

Marginal note:Minister’s approval

  •  (1) A holder of a licence for analytical testing must obtain the Minister’s approval before

    • (a) designating or replacing an alternate head of laboratory; and

    • (b) replacing the head of laboratory by an individual, other than by an alternate head of laboratory.

  • Marginal note:Application — content

    (2) The holder of a licence for analytical testing must, for the purpose of obtaining the Minister’s approval, submit an application that includes the following:

    • (a) the name and date of birth of the proposed alternate head of laboratory or the proposed head of laboratory;

    • (b) a description of the proposed head of laboratory’s or the proposed alternate head of laboratory’s qualifications in respect of the matters referred to in subsection 23(2); and

    • (c) a declaration, signed and dated by the responsible person referred to in section 37, indicating that all information provided in support of the application is correct and complete to the best of their knowledge.

  • Marginal note:Additional information

    (3) The Minister may, on receiving an application for approval, require the submission of any additional information that pertains to the information contained in the application and that is necessary for the Minister to consider the application.

Marginal note:Destruction

  •  (1) A holder of a licence for analytical testing must destroy all samples of cannabis of a lot or batch that have been distributed to them, and all cannabis obtained from those samples, within 90 days after completing the testing of the samples of the lot or batch.

  • Marginal note:Samples not tested

    (2) If testing of the samples of cannabis distributed to the holder of the licence for analytical testing is not initiated within 120 days of their receipt, the holder must destroy the samples within that period.

Licence for Sale for Medical Purposes

Marginal note:Authorized activities

 Subject to the other provisions of these Regulations, a holder of a licence for sale for medical purposes is authorized to conduct those of the following activities that are authorized by the licence:

  • (a) to possess cannabis products; and

  • (b) to sell cannabis products.

Marginal note:Sale — other than clients

  •  (1) Subject to subsection (2), a holder of a licence for sale for medical purposes that authorizes the sale of cannabis products is authorized to sell or distribute

    • (a) cannabis products to any of the following:

      • (i) a holder of a licence, other than a licence for cultivation,

      • (ii) the Minister, or

      • (iii) a person to which an exemption has been granted under section 140 of the Act in relation to the cannabis or class of cannabis that is, or is contained in, a cannabis product that is sold or distributed;

    • (b) dried cannabis, fresh cannabis, cannabis plants and cannabis plant seeds, that are cannabis products, to a holder of a licence for micro-cultivation or standard cultivation;

    • (c) cannabis plants and cannabis plant seeds, that are cannabis products, to a holder of a licence for a nursery; and

    • (d) cannabis products, other than cannabis plants and cannabis plant seeds, to a hospital employee if the employee’s possession of the cannabis product is for the purpose of, and in connection with, their duties.

  • Marginal note:Packaging

    (2) A holder of a licence for sale for medical purposes must sell the cannabis products referred to in subsection (1) in the packaging in which they were sold or distributed to the holder.

 
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