Re-evaluation Note REV2013-11, Re-evaluation Project Plan for Quinclorac
Pest Management Regulatory Agency
20 November 2013
ISSN: 1925-0649 (PDF version)
Catalogue number: H113-5/2013-11E-PDF (PDF version)
In Canada, quinclorac is under re-evaluation by Health Canada’s Pest Management Regulatory Agency (PMRA). The PMRA’s pesticide re-evaluation program considers potential risks as well as the value of pesticide products to ensure they continue to meet standards of modern science and current policy established to protect human health and the environment. Under the authority of Section 16 of the Pest Control Products Act, the registrants of quinclorac were notified of the initiation of the re-evaluation of quinclorac. Following this, the registrant of quinclorac technical grade active ingredient in Canada indicated their intention to support all uses included on the labels of commercial products in Canada. This Re-evaluation Note outlines a project plan and timeline for review, as well as summarizes the anticipated areas of focus related to the re‑evaluation of quinclorac.
Quinclorac is an herbicide that has been registered in Canada since 1997. Quinclorac is currently registered for selective post-emergence control of green foxtail, cleavers, volunteer flax, barnyard grass; suppression of annual and perennial sow thistle in spring and durum wheat, spring barley and canary seed in the prairie provinces and Peace River region of British Columbia only (Use-Site Category 7, 13 and 14). Registered quinclorac end-use products are formulated as wettable granules or water dispersible granules in water soluble packaging, to be applied by ground equipment only.
The project plan discussed below outlines the anticipated areas of focus and risk assessments required to complete the re-evaluation of quinclorac. Should additional information become available during the re-evaluation period that affects the regulatory status of quinclorac, the Agency will reconsider the areas of focus and risk assessments required. Currently, a proposed re-evaluation decision for quinclorac is anticipated to be published in 2015.
Re-evaluation Project Plan
Human Health Risk Assessment
The toxicology database for quinclorac was considered complete at the time of initial registration and no major updates have been made since then. Data generated since the time of the original submission (for example, additional acute toxicity studies, immunotoxicity, short-term inhalation and neurotoxicity studies) that may impact the hazard assessment, will be evaluated. Verification of the points of departure used for risk assessment will be undertaken and areas not addressed in the original evaluation (for example, establishment of an acute reference dose, application of the PCPA factor) will be reviewed. Recent scientific literature and incident reports will also be incorporated into the re-evaluation.
Dietary exposure and risk assessments previously conducted to support currently registered uses will be verified to ensure they meet current science standards and policies. This includes the incorporation of revisions to toxicological reference doses if applicable, drinking water estimated environmental concentrations, food consumption data and the use of available residue data from pesticide residue surveillance programs conducted by the Canadian Food Inspection Agency and the United States Department of Agriculture.
The occupational exposure and risk assessments will be revised to reflect the currently available scientific data and approaches, as well as revised toxicological points of departure, if applicable. In the absence of chemical-specific data, standard defaults will be used in the occupational exposure and risk assessment.
Environmental Risk Assessment
Environmental risk assessments will be updated, where appropriate, using current methodologies, available scientific data and relevant scientific literature.
Environmental risk mitigation measures will be reviewed to ensure consistency with current label requirements.
Buffer zones for the protection of sensitive terrestrial and aquatic habitats will be calculated based on current practices and taking into consideration currently registered uses.
The Toxic Substances Management Policy (TSMP) will be taken into consideration.
Environmental fate will be reviewed to determine drinking water and environmental EECs for risk assessment purposes.
The value of quinclorac will be considered. The viability of alternatives will be examined if risks of concern are identified.
Additional data requirements related to toxicology and environmental assessment have been identified for quinclorac and were requested from technical registrants (Appendix I).
Anticipated Timeline for Re-evaluation
A proposed re-evaluation decision for quinclorac is anticipated to be published for consultation in 2015.
PMRA documents can be found in the Pesticides and Pest Management section of Health Canada's website at healthcanada.gc.ca/pmra. PMRA documents are also available through the Pest Management Information Service. Phone: 1-800-267-6315 within Canada or 1-613-736-3799 outside Canada (long distance charges apply); fax: 613-736-3798; e-mail: email@example.com.
Appendix I - Data Requirements for the Re-evaluation of Quinclorac
- DACO 4.2.1 - Acute Oral
- DACO 4.2.2 - Acute Dermal
- DACO 4.2.3 - Acute Inhalation
- DACO 4.2.4 - Primary Eye Irritation
- DACO 4.2.5 - Primary Dermal Irritation
- DACO 4.2.6 - Dermal Sensitization
- DACO 4.3.7 - Short-term Inhalation (21/28 day)
- DACO 4.5.7 - Genotoxicity
- DACO 4.8 - Other Studies - Neurotoxicity and Immunotoxicity
- DACO 18.104.22.168 - Special Studies - Groundwater
- DACO 9.3.3 - Daphnia sp. Chronic (Life-Cycle)
- DACO 22.214.171.124 - Fish, Early Life Cycle Toxicity Test
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