Food and Drug Regulations
G.02.014 (1) Every licensed dealer shall keep a record of the following:
(a) the name and quantity of any controlled drug received by the licensed dealer, the name and address of the person who sold or provided it and the date it was received;
(b) the name, quantity and form of any controlled drug sold or provided by the licensed dealer, the name and address of the person to whom it was sold or provided and the date it was sold or provided;
(c) the name and quantity of any controlled drug used in the making or assembling of a product or compound containing that controlled drug, the name and quantity of the product or compound made or assembled and the date on which the product or compound was placed in stock;
(c.1) the name and quantity of any controlled drug produced and the date on which it was placed in stock; and
(d) the name and quantity of any controlled drug he had in stock at the end of each month.
(2) The record of information referred to in subsection (1) shall be kept
(a) in a manner that permits an audit to be made;
(b) subject to subsection (3), in a book, register or similar record maintained exclusively for controlled drugs; and
(c) for any period of at least two years on the premises described in the licence of the licensed dealer.
(3) The record of information referred to in paragraphs (1)(a), (b) and (d) may, with respect to a controlled drug listed in Part II or III of the schedule to this Part, be kept in a form other than that specified in paragraph (2)(b).
- SOR/78-427, s. 1
- SOR/97-228, s. 10
- SOR/2004-238, s. 6
- SOR/2010-222, s. 8(E)
- Date modified: