With regard to the recommendations in Health Canada’s publication through the National Advisory Committee on Immunization titled, “Vaccination and pregnancy: COVID-19”: (a) how do these recommendations differ from the May 27, 2025, announcement by the United States of America’s Health and Human Services, stating the COVID-19 vaccine would no longer be included in the Centers for Disease Control and Prevention’s recommended immunization schedule for healthy pregnant women and healthy children (herein referred to as “cohort”) citing “mixed data” on booster safety and efficacy for pregnant women while seeking stricter clinical trials for vaccine approvals in healthy individuals under 65; (b) did communications occur, related to the Health and Human Services announcement, between Health Canada, the National Advisory Committee on Immunization or the Public Health Agency of Canada and (i) Health and Human Services, (ii) the United States of America’s Food and Drug Administration, (iii) the United States’Centers for Disease Control and Prevention, (iv) the United Kingdom’s Medicines & Healthcare products Regulatory Agency, (v) the European Medical Agency; (c) if the answer to (b) is affirmative, what (i) were the dates of the communications, (ii) were the modes of communications, (iii) were the names and titles of people included in the communications, (iv) was the outcome; (d) to Health Canada's knowledge, did the Medicines & Healthcare products Regulatory Agency or the European Medical Agency agree with Health Canada’s recommendations for the administration of the COVID-19 vaccine to this cohort; (e) does Health Canada, the National Advisory Committee on Immunization or the Public Health Agency of Canada have mixed data regarding booster safety and efficacy of the COVID-19 vaccine in this cohort, and, if so, how does this impact the risk-benefit analysis; (f) is Health Canada , the Public Health Agency of Canada or the National Advisory Committee on Immunization including the same or different data than the United States of America’s Health and Human Services, Food and Drug Administration, and Centers for Disease Control and Prevention in the decision to continue recommending the COVID-19 vaccines for this cohort; (g) what clinical trials or data is Health Canada, the National Advisory Committee on Immunization and the Public Health Agency of Canada including in their decision that gives them confidence to continue recommending these vaccines that differs from the United States of America’s Health and Human Services, the Food and Drug Administration, and the Centers for Disease Control and Prevention; (h) is Health Canada planning to request stricter clinical trials for vaccine approvals in healthy individuals under 65 in the future, and, if not, why not; (i) if the answer to (h) is affirmative, what additional vaccine clinical trial requirements will be needed for approval; (j) are there plans to change the recommendations with respect to the COVID-19 vaccine in this cohort; and (k) if the answer to (j) is affirmative, when will these recommendations be announced, and what will they include?
House of Commons Hansard #21 of the 45th Parliament, 1st session. (The original version is on Parliament's site.) The word of the day was citizenship.