Dr. Jessica Rose - Apr 13, 2023 - Winnipeg, Manitoba

10 months ago
1.07K

Dr. Rose's research involves descriptive analysis of data using the US Vaccine Adverse Event Reporting System (VAERS). The COVID-19 injectable products were rushed to market via Emergency Use Authorization (EUA) and corners were cut in pre-clinical and clinical trials (only healthy people within a certain age requirement were able to participate in the phase 3 trials, placebo participants were unblinded and injected with the produce, thus losing a comparative group). The COVID-19 injectable products, especially the modified mRNA products, have not been proven safe or effective. There simply wasn't enough time to make any claims of long-term safety.

For the complete witness testimony, transcript, exhibits and more, please visit https://nationalcitizensinquiry.ca/witness/dr-jessica-rose

Testimony Code: 2304WPG101

Loading 2 comments...