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Human Pathogens and Toxins Act (HPTA)

Frequently Asked Questions and Answers


Q. What is the Human Pathogens and Toxins Act all about?

The purpose of the HPTA is to establish a safety and security regime to protect the health and safety of the public against the risks posed by human pathogens and toxins.  It will require all persons (subject to specified exemptions) in Canada conducting activities with human pathogens or toxins to operate under the same safety rules.  It is also about enhancing our national security, and protecting Canadians from the risks posed by anyone who would intentionally misuse these dangerous agents.

Types of Pathogens and Risk Groups

Q. What are human pathogens; what are toxins?

A human pathogen is a micro-organism, nucleic acid or protein capable of causing disease in a human. This includes animal or plant pathogens that can cause disease in humans. Toxins are substances that are produced by or derived from a microorganism which are able to cause disease in a human.

Q. How are human pathogens and toxins categorized under this Act?

Under this Act, human pathogens are divided into risk groups, as defined in Section 3. These definitions outline the criteria to be used in assessing which risk group a human pathogen may fall into. These criteria include the level of risk to the health of a person or to public health, as well as the likelihood that the human pathogen will cause disease in a human, and whether or not treatment and preventative measures are available.  Examples of human pathogens that fall into each Risk Group are provided in Schedules 2 to 4. Toxins are those listed in Schedule 1.

Q. How will the Agency determine what should be in Schedules 1 to 5? 

The Public Health Agency of Canada will establish an advisory committee to advise the Minister on the risk group classification of human pathogens and toxins and what should be in Schedules 1 to 5.  The advice of this committee will be made public.