PMPRB Update: Revised Compliance Timelines For Grandfathered And Gap Medicines And Proposed Regulatory Amendments Directed To CSPs

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Smart & Biggar

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Smart & Biggar uncovers and maximizes intellectual property and technology assets for our clients. Today’s fast-paced innovation economy demands a higher level of expertise and attention to detail when it comes to IP strategy and protection. With over 125 lawyers, patent agents and trademark agents collaborating across five Canadian offices, Smart & Biggar is trusted by the world’s leading innovators to find value in their IP rights. As market leaders in IP, Smart & Biggar’s team is on the pulse when it comes to the latest developments and the wider industry changes that impact our clients. To stay informed, visit smartbiggar.ca/insights, including access to our RxIP Update (smartbiggar.ca/insights/rx-ip-updates), a monthly digest of the latest decisions and law surrounding the life sciences and pharmaceutical industries.
On April 16, 2021, in view of COVID-19, the Patented Medicine Prices Review Board (PMPRB) reversed its position on compliance timelines for Grandfathered and Gap medicines: compliance with the...
Canada Food, Drugs, Healthcare, Life Sciences
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Revised compliance timelines for Grandfathered and Gap medicines

On April 16, 2021, in view of COVID-19, the Patented Medicine Prices Review Board (PMPRB) reversed its position on compliance timelines for Grandfathered and Gap medicines: compliance with the Maximum List Price for these medicines will now be assessed after two filing periods (previously one, see our article here). In the result, the operative date for assessing compliance for Grandfathered and Gap Medicines with the amendments coming into force on July 1, 2021 is now July 1, 2022.

Forward Regulatory Plan 2021-2023: proposed amendments to the Patented Medicines Regulations  and PMPRB Rules of Practice and Procedure

Pursuant to the CETA Implementation  Act, amendments to the Patent Act  relating to the PMPRB's jurisdiction over Certificates of Supplementary Protection (CSP) holders will come into force on a date to be fixed by order of the Governor in Council (s. 138(5)). The relevant amendments will define a "rights holder" as "a patentee and a person for the time being entitled to a [CSP] for that invention" (section 79(1)) and amend section 80(1) to require a rights holder to provide the PMPRB with pricing information (section 80(1)).

As part of its Forward Regulatory Plan for 2021-2023, which outlines regulatory initiatives for the next two years, Health Canada has announced its intention to amend both the Patented Medicines Prices Review Board Rules of Practice and Procedure  (plan here, with final amendments expected in winter 2021) and the Patented Medicines Regulations (plan here, with final amendments expected in spring 2021) to reflect the above expansion of the jurisdiction of the PMPRB to rights holders of CSPs. The amendments to the Patent Act are expected to come into force in the spring of 2021.

Should you have any questions, please do not hesitate to contact a member of the Life Sciences Regulatory & Compliance Group.

The preceding is intended as a timely update on Canadian intellectual property and technology law. The content is informational only and does not constitute legal or professional advice. To obtain such advice, please communicate with our offices directly.

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