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This guidance document explains the regulatory information requirements and conditions for practitioners and manufacturers when drugs are requested through the …
The Special Access Programme (SAP) allows practitioners to request access to drugs that are unavailable for sale in Canada. This …
Adoption of International Conference on Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use (ICH) Guidance Document: …
E9: Statistical Principles of Clinical Trials. This guidance has been developed by the appropriate ICH Expert Working Group and has …
The objective of this guidance document is to allow the compilation of a single core clinical study report acceptable to …
This dataset displays the Canadian geographic ranges of the priority species identified under the Pan-Canadian Approach for Transforming Species at …
Fisheries and Oceans Canada’s (DFO) National Biofouling Monitoring Program (BMP) has conducted annual field surveys to monitor the introduction, establishment, …
Access the List of Ambient Air Quality Criteria (AAQC) set by the Ministry of the Environment, Conservation and Parks. An …
Veterans Review and Appeal Board 2023 Accessibility Progress Report
This guidance document is intended to aid manufacturers and regulatory representatives in preparing medical device licence applications for dermal fillers.