Consultation: Annex 17 to the Good manufacturing practices guide - Real time release testing and parametric release (GUI-0046)

Current status: Open

Opened on September 10, 2024, and will close to new input on October 24, 2024.

Health Canada has released Annex 17 to the Good manufacturing practices guide – Real time release testing and parametric release (GUI-0046) for a 45-day stakeholder consultation period.

This guide is an annex to the Good manufacturing practices guide for drug products (GUI-0001). These guides are to be read together. They will help you understand and comply with Part C, Division 2, of the Food and Drug Regulations, which is about good manufacturing practices (GMP).

This revised guidance document contains new information with key changes listed below.

Join in: how to participate

If you wish to participate, you may obtain the consultation package by emailing us at hpil-consultation-ipsop@hc-sc.gc.ca.

You may send your comments to hpil-consultation-ipsop@hc-sc.gc.ca by October 24, 2024. We will consider all comments when we finalize the guidance document.

Key changes

The revised guidance document has been edited to make it easier to understand.

We have also made changes in several sections to make the meaning clearer. For example, we:

We also added a reference section that also includes relevant references from other jurisdictions, along with their URLs.

Contact us

Health Product Compliance Directorate (HPCD)
13th Floor, Jeanne Mance Building
200 Eglantine Driveway, Tunney's Pasture
Ottawa ON K1A 0K9
Email: drug.gmp.questions-bpf.medicaments@hc-sc.gc.ca

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