Compare

Compare archived captures

This view highlights text differences between two archived captures. It does not interpret meaning or provide guidance.

Descriptive changes only

This comparison highlights text changes between archived captures. It does not interpret the change or provide medical advice. For up-to-date recommendations, always consult the official source website.

Need to cite this comparison? See /cite.

Earlier capture

Consultation on draft guidance on co-packaged drug products: Share your views - Canada.ca

Apr 18, 2025

legacy-hc-2025-04-21

ID 147142

Later capture

Draft guidance on co-packaged drug products: Closed consultation - Canada.ca

Jan 2, 2026

hc-20260101

ID 428988

High-noise change

This change may include layout or boilerplate updates (such as navigation or footer adjustments). Treat the diff as descriptive, not definitive.

updated1 sections changed; 4 added; 7 removed (high-noise change)
1 sections changed4 added7 removed+11 / -27 linesChange ratio: 53%
---
+++
@@ -1,24 +1,19 @@
-Share your views: Consultation on draft guidance on co-packaged drug products
+Draft guidance on co-packaged drug products: Closed consultation
From:
Health Canada
-Current status: Open
-Opened on March 18, 2025, and will close to new input on May 18, 2025.
-Health Canada has drafted a guidance document on co-packaged drug products. This document explains the regulatory requirements for co-packaged drug products and their components. This draft guidance is open for consultation.
-Join in: how to participate
-Send us an email
-Send an email to
-bpsip-bpspiconsultation@hc-sc.gc.ca
-with your ideas or comments to make yourself heard.
-Participate by mail
-Send a letter with your ideas and input to the address in
-contact information
-below.
-Who is the focus of this consultation
-The Government of Canada would like to hear from all interested parties, including:
+Current status: Closed
+This consultation ran from March 18 to May 18, 2025.
+Health Canada has drafted a guidance document on co-packaged drug products. This document explains the regulatory requirements for co-packaged drug products and their components.
+Who was the focus of this consultation
+Health Canada engaged with interested parties, including:
manufacturers of co-packaged drug products and their components
manufacturers, importers and distributors of all classes of medical devices included in a co-packaged drug product
others involved in packaging, labelling, importing or selling co-packaged drug products
health care professionals and associations
+What we heard
+To view the summary report of the consultation, see
+What we heard: Draft guidance on co-packaged drug products
+.
Key points about the draft guidance
This draft guidance explains the regulatory requirements for co-packaged drug products and their components. It:
defines types of co-packaged products
@@ -29,16 +24,5 @@
Learn more:
Draft guidance on co-packaged drug products
Health Canada drafts guidance on co-packaged drug products: Notice
-Contact us
-Bureau of Policy, Science and International Programs
-Pharmaceutical Drugs Directorate
-Health Products and Food Branch
-Health Canada
-1600 Scott St
-Address Locator: 3106B
-Ottawa ON K1A 0K9
-Email:
-bpsip-bpspiconsultation@hc-sc.gc.ca
Page details
-Date modified:
-2025-03-18
+2025-10-27