Patented Medicine Prices Review Board
The Patented Medicine Prices Review Board (PMPRB) protects and informs Canadian consumers by reviewing the prices of patented medicines sold in Canada, and by reporting on pharmaceutical trends.
We are an independent quasi-judicial body that is part of the Health portfolio, and operate at arm’s-length from the Minister of Health.
Follow:
We are in the process of moving our services and information to Ca-ciconline.com.
Our current Patented Medicine Prices Review Board website will remain available until the move to Ca-ciconline.com is complete.
Latest news
Scoping paper for the consultations on the Board's Guidelines
Read the Scoping Paper and review the feedback that will help inform the development of the PMPRB Guidelines.
CompassRx, 9th Edition
This edition of the report focuses on the 2021/22 fiscal year, with a retrospective look at recent trends.
Most requested
Contact us
More information for
Services and information
Regulatory Process
Find information on the PMPRB’s regulatory and investigative process.
Information for patentees
Find information on the PMPRB's statutory reporting requirements, guidance on filing requirements and deadlines, outreach presentations and recorded Webinar sessions, and answers to frequently-asked questions.
Reports and Trends
Find information on key trends in sales and prices of patented medicines, and in pharmaceutical industry investments in research and development.
Voluntary Compliance Undertakings
See what patented medicines have been the subject of a pricing investigation that was resolued through a mutually acceptable pricing agreement between the PMPRB and the patentee.
National Prescription Drug Utilization Information System
NPDUIS is a research initiative jointly conducted by the PMPRB and the Canadian Institute for Health Information (CIHI).
Get answers to your questions
Find quick and direct answers to frequently asked questions
Legislation
The Patented Medicine Prices Review Board operates within the boundaries of various legislation, regulations and guidelines.
What we are doing
Corporate information
Management
Thomas J. Digby
Chairperson
Management
Vacant
Executive Director
Features
Regulatory Process
The PMPRB is responsible for ensuring the prices that patentees charge for prescription and non-prescription patented medicines sold in Canada to wholesalers, hospitals, pharmacies or others, for human and veterinary use, are not excessive.
NPDUIS Analytical Studies
Every report and publication published by the NPDUIS group.
Consultations
Effective and meaningful stakeholder involvement is essential to enable the PMPRB to fulfil its mandate, deliver programs, launch new initiatives, and build public trust.
Page details
- Date modified: