Madam Chair, as Minister Hajdu noted, the regulatory review based on clinical evidence provided by Pfizer indicated that the dose interval should be 21 days in the context of Pfizer authorization and 28 days in the case of Moderna. This regulatory authorization was then considered looking at the broader benefits and risks and the clinical evidence by the National Advisory Committee on Immunization in terms of the clinical guidance they provided.
Iain Stewart can speak to that in the context of the Public Health Agency, given their direct relationship with the National Advisory Committee on Immunization.