ARTICLE
31 March 2022

New Guidance Documents And Regulatory Amendments Regarding Therapeutic Product Shortages

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Smart & Biggar

Contributor

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.
As we have previously reported, in response to the COVID-19 pandemic, the Minister of Health had made interim orders pursuant to the Food and Drugs Act...
Canada Food, Drugs, Healthcare, Life Sciences
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As we have previously reported, in response to the COVID-19 pandemic, the Minister of Health had made interim orders pursuant to the Food and Drugs Act to address the significant risk to health posed by shortages in 2020 and 2021. In anticipation of the expiry of Interim Order No. 2, Regulations Amending Certain Regulations Concerning Drugs and Medical Devices (Shortages) (the "Regulations") were promulgated in 2021, with some provisions set to come into force later. Health Canada has issued a Notice regarding the Regulations, which includes an explanation of how the amendments differ from the previous now-expired interim orders.

On March 2, 2022, provisions of the Regulations regarding the following subjects, among others, came into force:

  • exceptional importation and sale of drugs and medical devices
  • amendment to the Certificate of Supplementary Protection Regulations  (to carve-out from the definition of "authorization for sale" permission to sell a drug under the Regulations)
  • mandatory reporting of shortages and discontinuations of specified medical devices and the power to compel information on medical device shortages

Health Canada has announced a new guidance for drugs: Guide to the exceptional importation and sale of drugs in response to drug shortages (GUI-0148). All products on the List of drugs for exceptional importation and sale, including existing products, will now have an end of importation date, but are allowed to be sold in Canada until the product expires.

Health Canada has also released related guidance documents for medical devices:

Additionally, on February 21, 2022, Health Canada made a further interim order re: medical devices: Interim Order No. 3 Respecting the Importation and Sale of Medical Devices for Use in Relation to COVID-19 (see our previous article about steps Health Canada has taken to facilitate availability of COVID-19 health products).

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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