• admin created the Catalogue Submit an application under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Declare identity and patent status of pharmaceutical product under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Declaring an attempt at negotiating a voluntary licence under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Declaring monetary value and units sold under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Renewal of licence under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Good faith clause under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Termination of authorization under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue How to comply with procedures under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Role of Non-Governmental Organizations in Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Anti-diversionary measures under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Capacity to manufacture under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Least-developed countries eligible to import under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue WTO-member countries and non-WTO member countries eligible to import under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Features of Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Regulatory Initiative: Amendments to the Food and Drug Regulations - Mandatory Reporting of Drug Shortages - Forward Regulatory Plan 2015-2017
  1 year ago
• admin created the Catalogue Improving the regulatory review of drugs and devices: Notice to industry - Aligned reviews between Health Canada and health technology assessment organizations
  1 year ago
• admin created the Catalogue Improving the regulatory review of drugs and devices: Early scientific advice to manufacturers
  1 year ago
• admin created the Catalogue Improving the regulatory review of drugs and devices: Expanding priority review pathways for drugs that meet health care system needs
  1 year ago
• admin created the Catalogue Improving the regulatory review of drugs and devices: Improving access to generic drugs
  1 year ago
• admin created the Catalogue Improving the regulatory review of drugs and devices: Drugs - Special Access to Drugs and Health Products
  1 year ago
• admin created the Catalogue Guidance Document: Administrative Processing of Submissions and Applications Involving Human or Disinfectant Drugs
  1 year ago
• admin created the Catalogue Public Release of Clinical Information: consultation
  1 year ago
• admin created the Catalogue Country access to Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Compulsory licences under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue WTO-member countries eligible to import under Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Guidance document on Public Release of Clinical Information: profile page
  1 year ago
• admin created the Catalogue Guidance Document: Considerations for Inclusion of Women in Clinical Trials and Analysis of Sex Differences
  1 year ago
• admin created the Catalogue Introduction to the Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Benefits for companies participating in Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Patent Act Schedules related to Canada's Access to Medicines Regime
  1 year ago
• admin created the Catalogue Regulating food
  1 year ago