As previously reported, in December 2024, Health Canada published its agile licensing amendments to the Food and Drug Regulations (FDRs). The amendments included authorities that will come into force on April 1, 2027, permitting Health Canada to (i) impose terms and conditions (T&Cs) on all drugs with a drug identification number (DIN) and (ii) consider whether T&Cs could address promising evidence on the effectiveness of a new drug intended for serious or severely debilitating diseases or conditions.
On December 12, 2025, Health Canada launched a consultation on two draft guidance documents relating to these new T&C authorities:
- Draft guidance on terms and conditions for human and veterinary drugs: This document provides guidance to manufacturers and Health Canada staff on the use of T&Cs in accordance with Part C, Division 1, section C.01.014.21 of the FDRs. While a draft guidance was first published in December 2022, Health Canada notes that the current draft has been substantially revised. (Consultation page)
- Draft guidance on human and veterinary drug submissions based on promising evidence and terms and conditions: This guidance focuses on new drug submissions based on promising evidence of clinical efficacy where T&Cs are considered pursuant to section C.08.003.2 of the FDRs. (Consultation page)
Once the new authority to impose T&Cs takes effect on April 1, 2027, it will replace the following policies provisions and guidance:
- Guidance Document: Notice of Compliance with Conditions (NOC/c) for human drugs
- T&Cs provisions in the FDRs that are specific to opioids (subsection C.01.014.21(1)) and public health emergency drugs (subsection C.01.014.21(1.1))
- Policy on terms and conditions for veterinary drugs
The consultation is open until February 10, 2026.
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 life sciences regulatory law. The content is informational only and does not constitute legal or professional advice. To obtain such advice, please communicate with our offices directly.
Related Publications & Articles
-
Health Canada’s modernization of clinical trial framework: notice of interim policy and results from consultation
As we previously reported, Health Canada consulted on the framework for clinical trials, including on the new Clinical Trials Regulations and draft and updated guidance documents. Health Canada has no...Read More -
Health Canada issues new and updated guidance for managing therapeutic product shortages
On October 7, 2026, Health Canada published a new Guide on extending expiration dates of marketed drugs in response to drug shortages (GUI-0500).Read More -
Health Canada provides its quarterly update and PMPRB publishes the 10th edition of the Meds Entry Watch report
On October 15, 2026, Health Canada provided its quarterly update summarizing steps it has taken “to make its regulatory processes more modern and efficient, while maintaining high standards for safety...Read More
