The review of the AstraZeneca submission is ongoing. We have gone through the bulk of the scientific information. This submission was a bit more complicated than the ones we've seen with Pfizer and BioNTech because of the way the data was collected.
We also note that different regulators are taking different approaches to how the AstraZeneca vaccine should be used. Currently, we're still going back and forth with the company with respect to some data. We just had some conversations with them today. It is in the final stages. That end process around the product monograph, the labelling, the indications, the risk management plan and the potential terms and conditions on the vaccine are still under discussion.
We know the European Medicines Agency has authorized the vaccine. The other largest regulatory authority, the U.S. FDA, is still waiting.