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Found 10 records similar to Regulatory Directive: Master Product/Master Copy Registration Process
The objective of this guidance document is to outline the procedures that veterinary Master File (MF) holders must follow to file confidential business information (CBI) directly with Health Canada's Veterinary Drugs Directorate (VDD) that is cross-referenced in support of an Applicant's veterinary drug submission (including DIN (Drug Identification Number) applications.)
The purpose of this document is to communicate a revised procedure for amending the Product Register to reflect a change in a registrant's name or a change in registrant.
This master list contains Parks Canada fees for services, facilities, products and rights and privileges as well as travel trade fees effective July 9, 2010. The user fees have been set consistent with the requirements of the User Fees Act and under the authority of the Parks Canada Agency Act. They apply to national parks, national historic sites and national marine conservation areas administered by Parks Canada. Also included are fees that have been or will be discontinued.
The purpose of this Regulatory Directive is to inform registrants, other interested parties and agencies about registration requirements for adjuvant products.
This directive outlines the requirements for the registration of microbial pest control agents and products proposed for pest management in Canada at this time.
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.
The purpose of this document is to inform pesticide registrants and other interested groups and agencies about the current regulatory status of chlorofluorocarbons (CFC's) under the authority of the Pest Control Products Act.
The purpose of this document is to inform registrants, user groups, government agencies and other interested stakeholders about the procedure for registering pesticides or amending registrations for emergency control of pest infestations where currently registered pesticides and non-chemical control methods or practices are insufficient to address the pest outbreak.
This Regulatory Directive outlines Health Canada's Pest Management Regulatory Agency (PMRA) policy on the regulation of formulants contained in pest control products (Part I). It also provides practical guidance to applicants and registrants on implementation of the Formulants Policy (Part II).
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.