Free trade agreements as they relate to the biopharmaceutical industryRead more
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Biomanufacturing and Life Sciences Strategy (BLSS) as it relates to the biopharmaceutical industry
Patented Medicines (Notice of Compliance) Regulations as it relates to the regulation of intellectual property for biopharmaceutical products
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Proposed pharmacare legislation related to any future national pharmacare program
Jocelyne Voisin · Senior Assistant Deputy Minister, Health Canada (HC)
Free trade agreements as they relate to the biopharmaceutical industryRead more
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Annual federal Budgets and Budget updates as it relates to the biopharmaceutical industry
Common Drug Review Policies as it relates to reimbursement recommendation decision-making process and framework
Proposed pharmacare legislation related to any future national pharmacare program
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Annual federal Budgets and Budget updates as it relates to the biopharmaceutical industryRead more
Proposed pharmacare legislation related to any future national pharmacare program
Free trade agreements as they relate to the biopharmaceutical industry
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulationsRead more
Annual federal Budgets and Budget updates as it relates to the biopharmaceutical industry
Proposed pharmacare legislation related to any future national pharmacare program
Common Drug Review Policies as it relates to reimbursement recommendation decision-making process and framework
Free trade agreements as they relate to the biopharmaceutical industry
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Free trade agreements as they relate to the biopharmaceutical industryRead more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Establish accountability with the federally financed Canadian Agency for Drugs and Technologies in Health (CADTH)
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Patented Medicines Regulations as it relates to the regulation and protection of biopharmaceutical productsRead more
Free trade agreements as they relate to the biopharmaceutical industry
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Establish accountability with the federally financed Canadian Agency for Drugs and Technologies in Health (CADTH)
Free trade agreements as they relate to the biopharmaceutical industryRead more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Establish accountability with the federally financed Canadian Agency for Drugs and Technologies in Health (CADTH)
Free trade agreements as they relate to the biopharmaceutical industryRead more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Establish accountability with the federally financed Canadian Agency for Drugs and Technologies in Health (CADTH)
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)Read more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Free trade agreements as they relate to the biopharmaceutical industry
Establish accountability with the federally financed Canadian Agency for Drugs and Technologies in Health (CADTH)
Gary Xie · Senior Policy Advisor to the Secretary of State, International Development, Global Affairs Canada (GAC)
Free trade agreements as they relate to the biopharmaceutical industryRead more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processesRead more
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulations
Free trade agreements as they relate to the biopharmaceutical industry
Proposed pharmacare legislation related to any future national pharmacare program
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Jocelyne Voisin · Senior Assistant Deputy Minister, Health Canada (HC)
Policy measures to ensure security of drug supply in Canada and preserve Canada's attractiveness for biopharmaceutical launches, including in response to foreign pricing regulationsRead more
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Free trade agreements as they relate to the biopharmaceutical industry
Policies and frameworks to accelerate access to innovative medicines post-Health Canada approval, including efforts to reduce time-to-reimbursement and streamline federal/provincial listing processes
Miro Froehlich · Director of Policy, for Minister responsible for Canada-U.S. Trade, Intergovernmental Affairs and One Canadian Economy, Privy Council Office (PCO)
Galen Richardson · Senior Advisor, Stakeholder Relations for Minister responsible for Canada-U.S. Trade, Intergovernmental Affairs and One Canadian, Privy Council Office (PCO)
Free trade agreements as they relate to the biopharmaceutical industryRead more
Pharmaceutical pricing policy issues arising from the jurisdiction of the Patented Medicines Prices Review Board (PMPRB)
Mélanie Joly · Minister of Industry and Minister responsible for Canada Economic Development for Quebec Regions, Innovation, Science and Economic Development Canada (ISED)
Free trade agreements as they relate to the biopharmaceutical industry
From the Office of the Commissioner of Lobbying's open data, published November 5, 2026.
Reports cover oral, arranged meetings with designated public office holders since November 22, 2021; lobbyists file them by the 15th of the following month.
Names of MPs are matched to the current House of Commons, and bills are linked when the lobbyist's own description makes clear which bill it means.
Contains information licensed under the Open Data Licence Agreement — Office of the Commissioner of Lobbying. Licence.
PolitiKit is independent and is not endorsed by the Commissioner of Lobbying.