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Controlled Substances Regulations (SOR/2025-242)

Regulations are current to 2026-03-17

Practitioners (continued)

Documents (continued)

Information (continued)

The following provision is not in force.

Marginal note:Written orders

 A practitioner who receives a written order must record the following information:

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    (a) their name; and

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    (b) the date of the order and the date on which it was received.

The following provision is not in force.

Marginal note:Transportation

 A practitioner who delivers, sends or transports a controlled substance must record the following information:

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    (a) their name and the name and municipal address of the place where they practise;

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    (b) if an agent or mandatary of the practitioner delivers, sends or transports the controlled substance, their name;

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    (c) if the controlled substance is delivered, sent or transported to another person, the following information with respect to that person:

    • (i) if they are an individual who is named in a prescription or who is responsible for an animal identified in a prescription, their name and, if applicable, the name of the animal,

    • (ii) if they are a consignee of a restricted drug, their name, or

    • (iii) in any other case, their name and, if applicable title;

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    (d) the municipal address of the place where the controlled substance is delivered, sent or transported;

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    (e) the date of the delivery, sending or transportation;

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    (f) in the case of a controlled substance set out in any of Schedules 1 to 4, its name, form and quantity; and

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    (g) in the case of a finished product,

    • (i) subject to subparagraph (iv), its name or, if applicable, brand name,

    • (ii) subject to subparagraph (iv), its form, strength and quantity,

    • (iii) subject to subparagraph (iv), its drug identification number, if any, and

    • (iv) if the finished product has been previously returned by an individual for the purposes of destruction, only the identifier marked on the collection container of the finished product and the number of collection containers.

The following provision is not in force.

Marginal note:Destruction

 A practitioner who destroys a controlled substance must record the following information:

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    (a) their name;

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    (b) the name of the witness to the destruction;

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    (c) the municipal address of the place of destruction;

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    (d) the date of destruction;

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    (e) the method of destruction;

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    (f) in the case of a controlled substance set out in any of Schedules 1 to 4, its name and quantity; and

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    (g) in the case of a finished product,

    • (i) subject to subparagraph (iii), its name or, if applicable, brand name,

    • (ii) subject to subparagraph (iii), its quantity, and

    • (iii) if the finished product has been previously returned by an individual for the purposes of destruction, only the identifier marked on the collection container of the finished product and the number of collection containers.

Recording Information and Retention and Provision of Documents

The following provision is not in force.

Marginal note:Method of recording

 A practitioner who records any information under these Regulations must do so using a method that permits an audit of it to be made at any time.

The following provision is not in force.

Marginal note:Documents to retain

 A practitioner who is responsible for the operations of a place where information was recorded under these Regulations or, if information was recorded at a place where operations have ceased, the person who was responsible for those operations on the date those operations ceased must ensure that

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    (a) any document containing the information that they are required to record under these Regulations is kept for two years after the day on which the last record is recorded in the document;

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    (b) every written order and prescription is kept, in sequence as to date and number, for two years after the day on which it is received or issued respectively; and

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    (c) every declaration, report and letter of authorization is kept for two years after the day on which it is provided or received.

The following provision is not in force.

Marginal note:Place

 The documents must be accessible

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    (a) at the place where the information was recorded; or

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    (b) if operations have ceased at that place, at a place in Canada.

The following provision is not in force.

Marginal note:Quality of documents

 The documents must be complete and readily retrievable and the information in them must be legible and indelible.

The following provision is not in force.

Marginal note:Providing documents

 A practitioner who is responsible for the operations of the place where the information was recorded or, if operations have ceased at a place where information was recorded, the person who was responsible for those operations on the date those operations ceased must provide any documents that the Minister requests in the time and manner that the Minister specifies.

Prescribed Practitioners

The following provision is not in force.

Marginal note:Additional conditions

 In addition to meeting any other requirements set out in these Regulations, the following practitioners who, in accordance with these Regulations and subject to section 154, conduct any activity with respect to a controlled substance, other than a restricted drug, may only do so if they are authorized by the provincial professional regulatory authority to conduct that activity:

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    (a) a midwife;

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    (b) a podiatrist; and

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    (c) a nurse practitioner.

The following provision is not in force.

Marginal note:Midwife and podiatrist

 A midwife or podiatrist must not possess or conduct any activity with respect to the following controlled substances:

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    (a) a narcotic set out in subitems 1(1) or (10), 2(1), 5(4) or 10(1) of Schedule 1; or

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    (b) a controlled drug set out in item 1 of Part 1 of Schedule 2, items 9 and 10 of Part 2 of that Schedule, or item 1 of Part 3 of that Schedule.

Hospitals

Application and General Conditions for Activities

The following provision is not in force.

Marginal note:Application

 For the purposes of sections 156 to 188, the terms pharmacist, pharmacy technician, intern and health professional, as defined in subsection 1(1), and practitioner, as defined in subsection 2(1) of the Act, are to be read as only including those who are practising in a hospital, except as otherwise provided.

The following provision is not in force.

Marginal note:Person in charge

 A person in charge of a hospital may permit another person to conduct an activity with respect to a controlled substance if

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    (a) in the case that the other person is a health professional, they are authorized by the provincial professional regulatory authority to conduct that activity; and

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    (b) the other person conducts that activity as part of their duties and functions.

The following provision is not in force.

Marginal note:Orders placed on behalf of hospital

 A person in charge of a hospital may only permit the following persons to order a controlled substance, other than a restricted drug, on the hospital’s behalf:

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    (a) a pharmacist; or

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    (b) a practitioner.

Sale of Controlled Substances

The following provision is not in force.

Marginal note:Sale to licensed dealer

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     (1) A hospital may sell or provide a controlled substance, other than a restricted drug, to a licensed dealer if

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      (a) in the case of a controlled substance previously returned by an individual for the purposes of destruction,

      • (i) the licensed dealer is specialized in destruction, and

      • (ii) the hospital first receives from that licensed dealer specialized in destruction a written order that is signed and dated and that contains the information set out in subsection (3); and

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      (b) in the case of any other controlled substance,

      • (i) one of the following conditions is met:

        • (A) the licensed dealer is the one that sold or provided that controlled substance to the hospital, or

        • (B) the hospital sells or provides the controlled substance for the purposes of testing or destruction, and

      • (ii) the hospital first receives from the licensed dealer a written order that is signed and dated and that contains the information set out in subsection (3).

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    Marginal note:Restricted drugs

    (2) A hospital may sell or provide a restricted drug to a licensed dealer if

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      (a) the restricted drug was previously returned by an individual for the purposes of destruction;

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      (b) the licensed dealer is specialized in destruction; and

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      (c) the hospital first receives from that licensed dealer specialized in destruction a written order that is signed and dated and that contains the information set out in subsection (3).

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    Marginal note:Written orders

    (3) The information that must be contained in the written order is the following:

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      (a) with respect to the licensed dealer, their name and, if applicable, title, as well as their municipal address;

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      (b) with respect to the hospital, its name and municipal address;

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      (c) the date of the order;

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      (d) in the case of a controlled substance set out in any of Schedules 1 to 3, its name, form and quantity;

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      (e) in the case of a finished product,

      • (i) subject to subparagraph (iv), its name or, if applicable, brand name,

      • (ii) subject to subparagraph (iv), its form, strength and quantity,

      • (iii) subject to subparagraph (iv), its drug identification number, if any, and

      • (iv) if the finished product has been previously returned by an individual for the purposes of destruction, only the identifier marked on the collection container of the finished product and the number of collection containers; and

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      (f) in the case of a controlled substance sold or provided for the purposes of destruction, a statement to that effect.

The following provision is not in force.

Marginal note:Sale to pharmacist

  • The following provision is not in force.

     (1) A hospital may sell or provide a controlled substance, other than a restricted drug, to a pharmacist, other than one who is practising in a hospital, if

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      (a) the sale or provision is in the case of an emergency; and

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      (b) the hospital first receives from the pharmacist either a written order that is signed and dated and that contains the following information or a verbal order:

      • (i) with respect to the pharmacist, their name and the name and municipal address of the place where they practise,

      • (ii) with respect to the hospital, its name and municipal address,

      • (iii) the date of the order,

      • (iv) in the case of a controlled substance set out in any of Schedules 1 to 3, its name, form and quantity,

      • (v) in the case of a finished product,

        • (A) its name or, if applicable, brand name,

        • (B) its form, strength and quantity, and

        • (C) its drug identification number, if any, and

      • (vi) a declaration from the pharmacist that they require the controlled substance for emergency purposes.

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    Marginal note:Exception — prohibition

    (2) A hospital must not sell or provide to the pharmacist a controlled substance that is the subject of a prohibition on the pharmacist’s professional practice imposed by the provincial professional regulatory authority.

 

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