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Food and Drug Regulations

Version of section C.08.011 from 2006-03-22 to 2020-09-27:

  •  (1) Notwithstanding section C.08.002, a manufacturer may sell to a practitioner named in a letter of authorization issued pursuant to section C.08.010, a quantity of the new drug named in that letter that does not exceed the quantity specified in the letter.

  • (2) A sale of a new drug made in accordance with subsection (1) is exempt from the provisions of the Act and these Regulations.


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