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Found 10 records similar to Regulatory Directive: Formulants Policy and Implementation Guidance Document
This dataset contains a list of formulants that are found in pest control products currently registered in Canada under the Pest Control Products Act and Regulations. This list is updated twice a year to reflect the addition of new formulants and the deletion of formulants no longer found in registered pest control products.
(This dataset was last updated on 2022-10-01)
The purpose of this Directive is to inform registrants, user groups, and other stakeholders about the Pest Management Regulatory Agency's strategy for the implementation of the Federal Government's Toxic Substances Management Policy (TSMP) for products regulated under the Pest Control Products Act.
This guidance document is specific to the "tamper-resistance" feature of controlled-release opioid products. It is intended for the pre-market review of drug submissions when sponsors seek to obtain approval for controlled-release opioid drug formulations with tamper-resistant properties and wish to include, in product monographs, scientific statements and claims regarding tamper-resistance.
The purpose of this document is to inform registrants and other interested groups and agencies about the colour standards for seed treatment products and the labelling requirements for treated seed. This document also outlines new labelling requirements for seed treatment products containing the formulant Rhodamine B.
The purpose of this Regulatory Directive is to inform registrants, other interested parties and agencies about the legislation and policy on the advertising of pest control products, and to provide some guideline on wording in promotional material and timing of advertising of control products.
The purpose of this document is to communicate to industry and other interested parties, revisions to the requirements for submitting documents to Health Canada's Pest Management Regulatory Agency (PMRA) in support of applications to register or amend a pest control product registration, re-evaluation or special review.
This regulatory directive outlines the Pest Management Regulatory Agency's (PMRA) re-evaluation program. It applies to technical active ingredients as well as to active ingredients in end-use products registered prior to December 31, 1994. The re-evaluation will include all end-use products associated with an active ingredient.
The purpose of this regulatory directive is to inform applicants, provinces and territories, user groups, and other interested parties that the North American Free Trade Agreement (NAFTA) Joint Review Programs for Reduced-Risk Pesticides will be extended by the Pest Management Regulatory Agency (PMRA) to include submissions made to the PMRA only.
In this Regulatory Directive, Health Canada's Pest Management Regulatory Agency (PMRA) describes new provisions for the protection of proprietary interests in data submitted to the PMRA in support of registration, re-evaluation and special review of pesticides, including technical grade active ingredients and their manufacturing concentrates as well as end-use products.
The aim of the regulation of pest control products is to ensure that pest control products offered for sale and use in Canada are safe to use, effective, and provide a demonstrated benefit or value. Value assessment is an important element of the pre-market evaluation of pest control products. Value assessments, as conducted by the Pest Management Regulatory Agency (PMRA), consist of three components: assessments of efficacy, of economic benefits and competitiveness, and of a pest control product's contribution to sustainability.