On
- Section 4 of the Amendments: specifying three new mandatory economic factors that the Board must consider when determining whether the price of a patented medicine is excessive and requiring patentees to report related information:
- The pharmacoeconomic value of the medicine;
- The size of the market for the medicine in
Canada ; and - The Gross Domestic Product (GDP) in
Canada and GDP per capita inCanada .
- Section 6 and the Schedule to the Amendments: changing the "basket" of comparator countries for the purpose of reference pricing; and
- Section 3(4) of the Amendments: providing a new price calculation requiring patentees to take into account discounts and rebates provided to third parties when reporting medicine prices to the Board.
The Court held that the first two impugned Amendments were intra vires the Patent Act, but the third Amendment (section 3(4)) was ultra vires.
The Court's analysis
The Court applied the recent
The Court held that a successful challenge to the vires of regulations requires a showing that the regulations are inconsistent with the objective of the enabling statute or the scope of the statutory mandate. A broad and purposive approach must be used to interpret both the challenged regulation and the enabling statute. This type of challenge does not involve assessing the policy merits of the regulations.
The Court cited the SCC's statements in
The Court held that the decision at issue is one made by the Governor in Council, which is separate from the Minister of Health. However, the Court also held that the Minister of Health's "comments describing modernizing the Board to 'lower the cost of drugs' are consistent with the explanation for the Amendments found in the RIAS, which states that the Amendments 'contribute to the Government's commitment [to improve the accessibility, affordability and appropriate use of medicines] by lowering the prices of patented medicines in
New mandatory economic factors
The Court agreed with the Respondent, holding that "assessing pharmacoeconomic value is an objective exercise using a standardized measure of benefit."7 The Court held that "[w]hile the patent monopoly allows patentees to price their products in a competition-free environment, patentees of medicines do not have unfettered pricing discretion. They must comply with
In making these findings, the Court also held that the Board must consider all of the factors found in s. 85(1) of the Patent Act. The Board cannot ignore one factor or allow a factor to dominate such that the other factors are rendered irrelevant. The new mandatory factors were held to complement the factors already found in s. 85(1). The Court dismissed arguments that the mandatory factors were limited in scope by s. 85(1) of the Patent Act, holding that s. 101(1) of the Patent Act does not limit the type of factors the Governor in Council may specify by way of regulation. The Court held that its view on whether the Amendments will succeed in achieving the statutory objectives is irrelevant.
The Court held that the new mandatory factors in s. 4 of the Amendments are within the scope of the Governor in Council's regulation-making authority, and thus the decision to promulgate this regulation is reasonable.
The "basket" of comparator countries
The Applicants acknowledged that the Governor in Council has the discretion to select the comparator countries; however, they argued that the basis upon which the new basket was selected conflicts with the purpose of s. 85(1) of the Patent Act. The Court disagreed, holding that "patentees of medicines do not have unfettered discretion to make their own pricing decisions in
The new price calculation
The new price calculation expands the information patentees must take into consideration when reporting the price at which the medicine is sold, requiring a reporting of price information net of discounts and rebates offered to parties further down the supply chain. The Applicants argued that this amendment exceeds the Board's factory-gate jurisdiction under the Patent Act. The Court agreed, holding that the Patent Act requires reporting on a sale by a patentee to a customer. Thus, any regulations must relate to the sale of medicines by patentees to customers.
The Court held that the Amendments in s. 3(4) are not limited to adjustments made by the customer or the patentee and extend to adjustments made by any party. "Requiring patentees to take into account financial transactions with third parties who are not customers - and are strangers to the original sale transaction - exceeds the scope of the Governor in Council's statutory mandate by untethering the price calculation from the sale of the patented medicine."10
The Court held that the Board's mandate is not to set prices for patented medicines and that the Board does not regulate profits made by patentees. "The Board's mandate to control prices is only engaged where it finds a patentee has abused its monopoly by charging excessive prices."11 The Court dismissed the Respondent's argument that the Applicants were making a constitutional argument with respect to this provision. The Court concluded that this provision was ultra vires the Patent Act.
Conclusions
The Court declared s. 3(4) of the Amendments invalid, void and of no force and effect. Section 4(4) of the Regulations as it currently reads will continue to operate. The remainder of the Amendments were held to be valid. The parties agreed not to seek costs regardless of outcome and thus, no costs were ordered.
Footnotes
1 Regulations Amending the Patented Medicines Regulations (Additional Factors and Information Reporting Requirements), SOR/2019-298 [the Amendments].
2 Patented Medicines Regulations, SOR/94-688 (the Regulations).
3
4 Innovative Medicines Canada, et al. v. The Attorney General of
5
6 IMC v. Canada, para 99; Regulatory Impact Analysis Statement, Canada Gazette Part II, Vol 153, No 17, pp5946-96 at 5949 (the RIAS)
7 IMC v. Canada, para 118.
8 IMC v. Canada, para 127.
9 IMC v. Canada, para 159.
10 IMC v. Canada, para 198.
11 IMC v. Canada, para 199.
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