Pest Control Products Incident Reporting Regulations

Marginal note:Section 13 of the Act

• 3 (1) The following information that is received by a registrant or an applicant about an incident that is associated with their pest control product or with any pest control product that has the same active ingredient, and that is required by sections 7, 8 and 16, is prescribed information for the purpose of section 13 of the Act:

  • (a) contact information for the registrant or applicant;

  • (b) the date on which the incident occurred;

  • (c) the date on which the registrant or applicant received the information about the incident;

  • (d) the city, province or state, and country where the incident occurred;

  • (e) the identification of the pest control product;

  • (f) information about the application of the pest control product, including the site, method and date of its application;

  • (g) the category of the incident, determined in accordance with section 2;

  • (h) information about the circumstances of the exposure to the pest control product, including the site, date, route of exposure, weather conditions, duration and subject information, which, in the case of a human subject, is restricted to age, gender and whether the subject is pregnant;

  • (i) information about the incident and its effects, including the symptoms, duration and outcome; and

  • (j) scientific test information, including information about the sample, the method of analysis and the results.

• Marginal note:Section 13 of the Act

  (2) The following information about an incident that is associated with the registrant’s or applicant’s pest control product or with any pest control product that has the same active ingredient, and that is required by section 9, is prescribed information for the purpose of section 13 of the Act:

  • (a) contact information for the registrant or applicant;

  • (b) the title and date of the study and the name of the author;

  • (c) the identification of the pest control product;

  • (d) the category of the incident, determined in accordance with section 2;

  • (e) the scientific study and the test data generated during the study; and

  • (f) the type of scientific study, an indication of which of subparagraphs 2(f)(i) to (iii) is the reason for submitting it, and the information the study reveals about the incident and its effects.