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Proposed Re-evaluation Decision PRVD2022-04, Corn gluten meal and its...
Corn gluten meal is registered as a herbicide on turf grass, residential lawns, municipal and commercial properties, golf courses, sports fields, parks and sod farms for pre-... -
Federal Contaminated Site Risk Assessment in Canada: Supplemental Guidance...
This guidance document was prepared to provide guidance to custodians of federal contaminated sites. -
Consultation: Draft technical document guidelines for Canadian drinking...
Health Canada is updating its guidance document on antimony in drinking water. We're looking for comments from regulatory authorities, decision makers and the public on the... -
Notice of clarification to drug manufacturers and sponsors:...
We are issuing this notice to help drug manufacturers and sponsors when preparing the Canadian-specific considerations and elements in the risk management plans (RMPs) for... -
Proposed Re-evaluation Decision PRVD2021-06, Difenoconazole and Its...
This document (Proposed Re-evaluation Decision PRVD2021-06, Difenoconazole and Its Associated End-use Products) presents the proposed re-evaluation decision for difenoconazole. -
Declaring an attempt at negotiating a voluntary licence under Canada's...
The pharmaceutical company must complete and submit to the Commissioner of Patents a Solemn or Statutory Declaration Under Paragraph 21.04(3)(c) of the Patent Act. The form sets... -
Drugs and vaccines for COVID-19
How Health Canada is addressing clinical trials of drugs and vaccines, its expedited review process and the Special Access Program to find therapies to prevent or treat COVID-19. -
The Safety of Food Additives
Food additives are chemicals that manufacturers or processors add to foods for various reasons, such as to preserve foods or improve their appearance. Although food additives... -
Guidance Document - Topical Anaesthetic/Analgesic/Antipruritic Labelling Standard
This labelling standard describes the requirements necessary to receive marketing authorization (a Drug Identification Number (DIN) or a Natural Product Number (NPN)) for... -
Registration Decision RD2022-09, Tiafenacil, Tiafenacil 70WG Herbicide,...
The Proposed Registration Decision PRD2022-01, Tiafenacil, Tiafenacil 70WG Herbicide, Tiafenacil 339SC Herbicide. -
Notice of danger to human health or safety and risk mitigation for Class 3B...
Health Canada has assessed the hazards associated with the use of handheld portable lasers of Class 3B or Class 4. These products may pose an eye injury hazard to children,... -
Subsection 56(1) class exemption for patients, practitioners and pharmacists...
Pursuant to subsection 56(1) of the Controlled Drugs and Substances Act (CDSA), and subject to the terms and conditions herein, practitioners and pharmacists, authorized within... -
About Natural Health Products
Health Canada information for the public on natural health products -
Regulatory Directive: Colour Standards for Seed Treatment Products and...
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... -
Compliance Verification Project 2021-2022: Toys Regulations (Magnets)
The purpose of this Compliance Verification (CV) project was to verify compliance of toys with specific magnetic force requirements of the Toys Regulations. -
Summary Safety Review - ZOFRAN (ondansetron) - Assessing the Potential Harm...
Health Canada carried out a safety review to assess the risk of birth defects with the use of ondansetron, as part of routine health product monitoring and because this drug is... -
Submissions Containing Clinical Data from Studies Conducted outside of Canada
Drug development is becoming increasingly global and Health Canada is receiving clinical studies submitted in support of a Canadian market authorization that are conducted... -
Request for disclosure of confidential business information (CBI)
Why we disclose confidential business information, who is eligible to request it and how to submit a request. -
Consumer Product Enforcement Summary Report - Cyclical Enforcement Project...
The purpose of this Cyclical Enforcement (CE) project was to verify the used-product industry’s compliance under the CCPSA and its regulations, the FDA, as it relates to...