With regard to Health Canada’s (HC) approval of mRNA vaccines for pregnant and lactating women, and children, youth, and adults of reproductive age: (a) what is the cause of the reported menstrual irregularities in vaccinated women; (b) what is the safety data on any single exposure and repeated exposure to lipid nanoparticles (LNP) for (i) pregnant women, (ii) unborn fetuses; (c) do LNPs, spike protein encoding mRNA, or spike protein pass through the placenta; (d) if the answer to (c) is affirmative, does this present a safety concern to the unborn fetus, and how was this determined; (e) where are LNPs, mRNA, or spike protein distributed in the fetus; (f) what are the potential genetic effects of the COVID-19 vaccine with respect to the epigenetic effects on germ cells; (g) what are the specific references confirming that mRNA is not integrated into the genome or genetic material of the oocyte or the sperm; (h) how, and for how long, does HC actively monitor or plan to actively monitor the impact of the dose-dependent effect of the vaccine on future fertility in (i) vaccinated women and men of child-bearing age, (ii) vaccinated children, (iii) children exposed in utero to the COVID-19 vaccines following maternal injection; (i) does HC actively monitor or plan to actively monitor the adverse effects of the mRNA vaccination, and for how long, in the (i) pregnant mother, (ii) fetus; (j) if the answer to (i) is affirmative, does this or will this include miscarriages, uterine deaths, possible illnesses and birth malformations; (k) with respect to studies analyzing various components and products of COVID-19 vaccination, including spike protein, what have been the findings comparing placental tissue and breast milk from vaccinated and non-vaccinated mothers, and what are the specific references; (l) based on available research and real-world data, what updated written guidance has HC provided to provinces and territories regarding information which is given to pregnant women prior to and after vaccination, their doctors (neonatal doctors, paediatricians, fertility doctors, obstetricians), other medical staff (including midwives), and vaccinators with respect to (i) the potential adverse events to monitor post-injection, (ii) their duty to report adverse events and where; and (m) does the guidance in (l) include the updated mRNA vaccine monographs and where to find them?