Colin Carrie on Questions Passed as Orders for Returns

With regard to the government authorization of mRNA COVID-19 vaccines: (a) when did Health Canada (HC), the Public Health Agency of Canada (PHAC), and the National Advisory Committee on Immunization (NACI), receive documentation from Pfizer acknowledging the presence of SV40 enhancer promoter sequence and SV40 poly(A)tail signal sequence in their vaccine BNT162b2; (b) with respect to the documentation related to (a), (i) how can the documentation be accessed, (ii) when was it received by HC, PHAC and NACI, (iii) was this documentation obtained before or after the BNT162b2 vaccine was authorized; (c) has HC asked Pfizer about the safety of the SV40 enhancer promoter sequence and SV40 poly(A)tail signal sequence in their vaccine, and, if not, why not; (d) if the answer to (c) is affirmative, what are the risk analyses that Pfizer did, if any, regarding these SV40 sequences; (e) what amount of SV40 sequences is considered safe (i) in a single Pfizer mRNA vaccine dose for distinct age groups, (ii) for repeated vaccine injections over time per each age group considered; (f) what were HC’s regulatory guidelines surrounding SV40 sequences in a vaccine prior to 2019; (g) what are the current (relevant for the period of 2019-2024) regulatory guidelines surrounding SV40 sequences in a conventional vaccine and in an mRNA vaccine; (h) how does HC know the SV40 fragments are inactive and have no functional role in mRNA vaccines; (i) has HC verified the amount of SV40 enhancer promoter sequence and SV40 poly(A)tail signal sequence in any of the Pfizer or Moderna mRNA vaccines, including the Pfizer XBB, and, if not, why not; (j) if the answer to (i) is affirmative, what was the outcome of this verification and how was this verification done; (k) what is HC’s official position with respect to the increased risk of DNA contaminants getting into human cells, including the cell nucleus, when encapsuled in liposomes, as is the case with the mRNA vaccines; (l) how has HC confirmed with certitude there is no genetic integration (i.e. in vivo transfection into the nucleus of human cells) of DNA plasmid fragments, which may or may not contain SV40 sequences, as found in either mRNA vaccine; (m) does the publicly undisclosed presence of SV40 sequences or any other adulteration (e.g. reverse open reading frames [ORF]) violate the terms and conditions of the Pfizer and Moderna contracts, and, if not, why not; and (n) if the answer to (m) is affirmative, what are the consequences?