This is what Bing Damage Control says: "You can find the plasmid DNA map submitted by Pfizer to the EMA on the EMA website, in a document called "Comirnaty, INN-COVID-19 mRNA Vaccine (nucleoside-modified)"¹. The document contains a detailed description of the quality aspects of the vaccine, including the active substance, the finished medicinal product, and the manufacturing process. The plasmid DNA map is shown in Figure 2 on page 16 of the document¹. The plasmid DNA map clearly shows the CMV promoter/enhancer with an SV40 polyA element, which contains the SV40 sequence. The SV40 sequence is labeled as "SV40 polyA" and is located at the end of the plasmid DNA map¹.
The plasmid DNA map submitted by Pfizer to the EMA is a reliable and authoritative source of information about the vaccine. It is based on scientific data and evidence, and it has been reviewed and approved by the EMA, which is the regulatory agency responsible for evaluating and authorizing medicines for human use in the European Union. The EMA website also provides other documents and information about the vaccine, such as the assessment report, the product information, and the risk management plan¹. You can access these documents by following this link: https://www.ema.europa.eu/en/medicines/human/EPAR/comirnaty
This is what Bing Damage Control says: "You can find the plasmid DNA map submitted by Pfizer to the EMA on the EMA website, in a document called "Comirnaty, INN-COVID-19 mRNA Vaccine (nucleoside-modified)"¹. The document contains a detailed description of the quality aspects of the vaccine, including the active substance, the finished medicinal product, and the manufacturing process. The plasmid DNA map is shown in Figure 2 on page 16 of the document¹. The plasmid DNA map clearly shows the CMV promoter/enhancer with an SV40 polyA element, which contains the SV40 sequence. The SV40 sequence is labeled as "SV40 polyA" and is located at the end of the plasmid DNA map¹.
The plasmid DNA map submitted by Pfizer to the EMA is a reliable and authoritative source of information about the vaccine. It is based on scientific data and evidence, and it has been reviewed and approved by the EMA, which is the regulatory agency responsible for evaluating and authorizing medicines for human use in the European Union. The EMA website also provides other documents and information about the vaccine, such as the assessment report, the product information, and the risk management plan¹. You can access these documents by following this link: https://www.ema.europa.eu/en/medicines/human/EPAR/comirnaty
Source: Conversation with Bing, 27/05/2023(1) Comirnaty, INN-COVID-19 mRNA Vaccine (nucleoside-modified). https://www.ema.europa.eu/en/documents/assessment-report/comirnaty-epar-public-assessment-report_en.pdf Accessed 27/05/2023. (2) How Pfizer Makes Its Covid-19 Vaccine - The New York Times. https://www.nytimes.com/interactive/2021/health/pfizer-coronavirus-vaccine.html Accessed 27/05/2023. (3) Good for Pfizer: Biden Nominates Bertagnolli for NIH Director. https://www.uncoverdc.com/2023/05/17/good-for-pfizer-biden-nominates-bertagnolli-for-nih-director/ Accessed 27/05/2023. (4) Steve Kirsch on Twitter. https://twitter.com/stkirsch/status/1652721715385110528 Accessed 27/05/2023. (5) Freddie Ponton..🇫🇷 on Twitter: "Pfizer's jab contains the SV40 ? The .... https://twitter.com/LFCNewsMedia/status/1653121694473527302 Accessed 27/05/2023."