Participation in consultations regarding the Digital Charter and the federal government's plans to overhaul Canada's privacy regime, to enable the use of anonymized health data for new medication research and development.
Raise awareness regarding the potential risks to drug and vaccine supply for Canadian patients arising from new U.S. state-level reimportation legislation.
Policies or Program
Engagement with government officials on disruptions to business, health & safety requirements, and opportunities to help with the COVID-19 pandemic.
Ensure the National Advisory Committee on Immunization has sufficient resources to undertake timely reviews of new vaccines that are made available to the Canadian marketplace.
Harmonizing rules for the sampling of natural health products under the proposed Canada-United States-Mexico trade agreement.
Input on the work of the Advisory Committee on the Implementation of National Pharmacare, specifically as it relates to access to medicines.
Renewal of national vaccine strategy to close gaps in vaccination coverage for Canadians, especially among seniors.
Sharing information with government and Members of Parliament on different models for national pharmacare, specifically as it relates to access to medicines.
The Government of Ontario has passed legislation requiring the public disclosure of payments made to Health Care Providers and Health Care Organizations by the broader health care industry, including pharmaceutical companies, generic manufacturers, and medical device companies. GlaxoSmithKline seeks to advocate for a national approach to disclosure through either the support of similar provincial initiatives, coordinated action through the Federal / Provincial and Territorial meetings of the Ministers of Health, and / or the establishment of national requirements.
Regulation
Allow for the regulation of products containing cannabidiol (CBD) as natural health products.
Engaging Health Canada on the Self-Care Products Initiative as it pertains to plain language labelling and a risk-based approach to regulatory oversight for non-prescription drugs.
Reforms to the Patented Medicines Review Board (PMPRB), whose guidelines seek to ensure a balance between the prices set by manufacturers for patented medicines sold in Canada and the maintenance of an attractive environment for pharmaceutical research and development. Specifically with regard to ensuring that any actions and proposed changes by the PMPRB do not negatively impact access to patented medicines in Canada.