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Ontario Public Drug Programs
In 2006, the government committed to reforming the public drug system through the Transparent Drug System for Patients Act, 2006, which made changes to the Ontario Drug Benefit Act and the Drug Interchangeability and Dispensing Fee Act. The Act enables the implementation of the government’s plan to create a stronger, more effective system in five key areas
- Improving patient access to drugs
- Ensuring better value for money
- Promoting the appropriate use of medications
- Investing in innovative health system research
- Strengthening the transparency and accountability in the public drug system
Ontario Public Drug Programs was formally established in April 2007, led by an Executive Officer and with staff from the former Drug System Secretariat and Ontario Drug Programs Branch. Legislation gives the Executive Officer a number of powers that previously resided with Cabinet and the Minister, including the mandate to :
- Administer the Ontario Public Drug Programs
- Keep, maintain and publish the Formulary
- Make the Act apply regarding the coverage of drugs that are not
listed drug products as provided through the exceptional access program
(Section 16 of the Ontario Drug Benefit Act (ODBA)).
- Designate products as listed drug products, listed substances and
designated pharmaceutical products and to remove and modify those
designations
- Designate products as interchangeable with other products under the
Drug Interchangeability and Dispensing Fee Act and to remove or modify those
designations
- Negotiate agreements with manufacturers of drug products, agree with
manufacturers as to the drug benefit price of listed drugs, negotiate drug
benefit prices for listed substances and set drug benefit prices for
designated pharmaceutical products
- Make payments under Ontario Public Drug Programs
- Establish clinical criteria under Section 23 of the ODBA
- Pay operators of pharmacies for professional services and
determining the amount of payment.
These changes will make the public drug system more efficient by allowing the Executive Officer to:
- Make faster decisions that are more responsive to patients, prescribers and manufacturers
- Communicate decisions and rationale publicly
- Partner with manufacturers to improve the process for listing drugs
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