Food and Drug Regulations
C.08.010 (1) The Director may issue a letter of authorization authorizing the sale of a quantity of a new drug for human or veterinary use to a practitioner named in the letter of authorization for use in the emergency treatment of a patient under the care of that practitioner, if
(a) the practitioner has supplied to the Director information concerning
(b) the practitioner has agreed to
(1.1) The Director shall not issue a letter of authorization under subsection (1) for a new drug that is or that contains a restricted drug as defined in section J.01.001.
(2) The Director shall, in any letter of authorization issued pursuant to subsection (1), state
- SOR/2013-172, s. 11.
- Date modified: