On August 27, 2020, approximately 4 months before the COVID-19 vaccines were rolled out in the USA, the CDC awarded General Dynamics Information Technology Inc. (GDIT) a contract for $35.4 million to support the CDC & FDA with collecting and analysing the Vaccine Adverse Events Reporting System (VAERS) data received post COVID-19 vaccine rollout. [1]
ICAN lawyers in 2023 received copies of the contract. It states that of the 45,500 average annual US reports received between 2014-2018, 5.0% were classified as serious…but in the contract the CDCexpected to receive “1,000 reports per day, with up to 40% of the reports serious in nature”, around a 700% increase in the daily reports for the SARS-CoV-2 vaccine! What did the CDC know about the imminent jab?
On Oct 22, 2020 Tom Shimabukuro presented CDC’s “plans for Vaccine Safetymonitoring & evaluation during future EUA use and post-licensure, suggesting that processing reports which included reviewing, coding and incorporating into VAERS’ database, was expected to take 1-5 business days – the fastest for death or serious reports. [2]
As part of their contract GDIT sends monthly reports to the CDC, which were received under FOIA in 2023. By January 2021 the report exceeded the maximum 1000/day, which was exceeded in the first 5 days of rollout! [3]