Drugs - Resources

Here you will find several sources of information on orphan drugs and on drugs in general.

Health Canada evaluates and authorizes all drugs for sale in Canada. For more information, see: How drugs are reviewed in Canada . To find information regarding drugs and other medical products in Canada, visit the page Drugs and health products .

For access to a drug that is not authorized by Health Canada, there is a program called the Special Access Program.

Quebec

Evaluation of a drug to determine if it will be reimbursed

In Quebec, it is the Institut national d’excellence en santé et en services sociaux (INESSS) which evaluates drugs for reimbursement by Quebec’s Public Prescription Drug Insurance Plan. These drugs must be authorized by Health Canada or in the process of being authorized.

Drug evaluation process and criteria used by INESSS: the evaluation framework was updated in July 2018. See also the Notice to the Minister published in November 2018 which speaks of a « paradigm shift » for the evaluation of certain innovative drugs with a « promise of therapeutic value ». This may apply to the evaluation of drugs for rare diseases.

  • To find a drug currently being evaluated or that has been evaluated: INESSS: Drugs products undergoing evaluation and evaluated Recommendations relating to drugs evaluated for registration purposes by INESSS are published regularly in a Notice to the Minister presented to the Minister of Health and Social Services.

**** Note that INESSS invites citizens, patients, caregivers, and healthcare professionals, as well as their associations and groups, to take part in the consultation on drugs that will be the subject of a scientific evaluation to determine if they should be reimbursed.The RQMO helps patients and caregivers participe in this evaluation process See here >>>>

Lists of drugs reimbursed in Quebec:

Other general information:

Other provinces and territories

It is Canada’s Drug Agency (CDA) which evaluates and makes recommendations for drug reimbursement in provinces and territories other than Quebec. To learn about the process, see: Reimbursement Reviews Process in Brief

***** Note that patient organizations may provide comments during CDA’s review of a drug: Stakeholder Feedback | CDA

For more information on orphan drugs and the RQMO’s services on this subject, consult this page.

Health Canada does not have a separate database for orphan drugs. You must consult its general database for all medications: Drug Product Database .

To find out if there is an orphan drug on the market or in development elsewhere in the world, consult the following sites:

Quebec

  • Changes to the evaluation of innovative drugs for rare diseases took place at INESSS in 2018. See the introduction to this INESS report on a drug for Fabry disease.
  • In the Quebec Action Plan for Rare Diseases 2023-2027:
    • “Objective 2.3 Improve access to care for people with
      a rare disease causing oral consequences”, including the establishment of a reimbursement program for oral care costs.
    • “Objective 2.4 Continue efforts to improve access to care and
      pharmaceutical services”, including: improving the offering of the Quebec Food Program for the treatment of hereditary metabolic diseases; optimizing access to stable blood products not distributed by Héma-Québec

Canada

Other countries

  • Find a clinical trial: see our “Research” page
  • Understanding Drug Research and Development: Eupati Toolbox
  • Patients at heart : to understand what a clinical trial is and help make the decision whether or not to participate in a clinical trial.

The RQMO has adopted policies governing relations with commercial companies, including those in the pharmaceutical industry:

See the Code of Ethics developed by Innovative Medicines Canada for its member companies and which sets standards for relations with health professionals, professional associations and patient associations.

Article: Principles for interactions with biopharmaceutical companies: the development of guidelines for patient advocacy organizations in the field of rare diseases – PMC (nih.gov)

Want to know if there is an orphan drug in development or on the market for your rare disease?

Contact us.

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