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Common Drug Review

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  • » CDR Overview

CDR Overview

Reducing duplication and maximizing resources

Prescription drugs are the fastest growing component of the Canadian health care budget. This increases the financial pressure on public drug plans.

Before the creation of the Common Drug Review (CDR), Canada’s federal, provincial, and territorial drug plans had separate processes for conducting reviews and making formulary listing recommendations.

The CDR was set up to reduce duplication, and provide equal access to high level evidence and expert advice, thereby contributing to the quality and sustainability of Canadian public drug plans. (All plans participate in CDR, except Québec.)

The CDR also consolidates the submission process for pharmaceutical manufacturers.

Objective, rigorous reviews, and evidence-based recommendations

The CDR helps support and inform drug plan decisions about drugs by providing:

  • systematic reviews of the clinical evidence
  • reviews of the pharmacoeconomic information
  • detailed recommendations by the Canadian Expert Drug Advisory Committee (CEDAC).

Drug plan decisions

The drug plans continue to make final benefit-listing and coverage decisions, based on CEDAC recommendations, and jurisdictional factors, such as plan mandates, priorities, and resources.

Background

The Common Drug Review is part of the Canadian Agency for Drugs and Technologies in Health. In March 2002, the CDR Directorate was established, and work to develop the CDR process started. The CDR began accepting submissions in September 2003.

Related Information

  • CDR Process
  • Advisory Committees
  • CADTH Common Drug Review: Myths and Facts
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  • CDR Evaluation

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Last Updated April 6, 2010