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PMPRB Fundamentals
Our next semi-annual "PMPRB Fundamentals" seminar will be held in
spring 2009.
Outline
A detailed, day-long learning session that provides an introduction to the Patented Medicines Prices Review Board and a basic understanding of its rules and principles. Topics covered include:
- Drug Categorization
- Scientific Reviews
- Price Reviews
- Submissions
- Data filing
The session provides answers to the following questions:
- How can I optimize the price of a new drug?
- How will my new drug be categorized?
- How much of an increase can I take on my price next year?
- When should I make a submission to the Board and when can I expect a response?
- What happens if my price exceeds the allowable price?
- When and what data should I be filing?
Why should you attend?
For a solid understanding of the PMPRB Fundamentals, it is best to learn it directly from the experts!
Brogan Inc. has been consulting with the pharmaceutical industry on Patented Medicine Prices Review Board [PMPRB] issues for over 15 years. Our vast experience, backed by detailed knowledge of the Patent Act and the Board's Guidelines, includes:
- New drug submissions
- Data filing
- Compliance strategies
Who should attend?
The seminar is useful to anyone involved in strategic pricing issues, PMPRB submission preparation, and in-licensing of patented medicines, including:
- Product Managers
- Pricing Managers
- New Product Development Managers
- Financial Officers/Controllers
- Government Affairs Managers
- Business Development and Strategy Managers
For more information, regarding this seminar, contact us at 613.599.0711, extension 255.
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