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WASHINGTON (PRWEB) April 20, 2020
Today, Ingersoll Lockwood, Inc. has announced the acquisition of the Cyber Defense Media Group, which it will fold into its portfolio in the coming months.
"Nothing in how CDMG operates will change with the exception of continued growth and additional focus on American Exceptionalism while we help spin out additional platforms for the Global commercial and international sectors in the coming months," said James Gorman, Vice Chairman of Ingersoll Lockwood.
"This is an incredible time for us and I'm especially excited to be able to help other divisions of Ingersoll Lockwood as they solve complex problems in different market sectors including cybersecurity, health care, critical infrastructure, big data, a.i. and space. This also gives me a chance to help cross pollinate activities and investments that we're doing in Stony Lonesome Group, where we focus exclusively on investing in US Military Veteran run startups," said Gary S. Miliefsky, Chairman & CEO of Cyber Defense Media Group and Publisher of Cyber Defense Magazine.
Miliefsky is a Founding Member of the US Department of Homeland Security (www.DHS.gov...), the National Information Security Group (www.NAISG.org...) and the OVAL advisory board of MITRE responsible for the CVE Program (CVE.mitre.org...). He also assisted the National Infrastructure Advisory Council (NIAC), which operates within the U.S. Department of Homeland Security, in their development of The National Strategy to Secure Cyberspace as well as the Center for the Study of Counter-Terrorism and Cyber Crime at Norwich University.
Previously, Gary has been founder and/or inventor for technologies and corporations sold and licensed to Hexis Cyber, WatchGuard, Intel/McAfee, IBM, Computer Associates and BlackBox Corporation.
“In fact, looking at their team, their patents, their experience, we now have a credible analysis that as I predicted, the Algorithms being used in the Dominion Voting System is intentionally and purposefully designed to create systematic fraud and influence election results and in this case, not in the favor of President Trump,” he added.
originally posted by: tallcool1
a reply to: F2d5thCavv2
Thanks Cav! The Kim Shady stuff does look interesting, but I still just don't get it. I can see some of the obvious stuff happening out there, but I suppose I'm not enough of an autist to discover all the sooper dooper secret clues and I can't find the secret decoder ring I got from my Cap'n Crunch.
If this Kim Shady (and other random social media accounts that are somehow "important") are part of the whole Q/KU/QUE/KYOO/etc. process, then I just don't understand - nor do I understand why someone (or some group of people) would put out "clues" (crumbs) that are so impossibly convoluted that no one can ever see through all the obfuscation to get to the truth! Seriously, someone "in the know" on twatter/darpabook/instacrap/etc posts a picture - but there's a random street sign in the background that points to some Kyoo post, but there was also a clock in the picture which points to another post - and it's raining in that post so watch the water...
This isn't directed at you Cav - nor at anyone else here in these threads. It just feels sometimes like the whole Kyoo thing has ended in failure, but we keep it going with wildly far-fetched "connections".
Obviously I'm still following these threads and I do still have about 5% hopium flowing through my veins, but ever since kyoo stopped posting it feels like it's just turned into some bizarre treasure hunt for hidden clues or something.
Audience: Individuals Performing COVID-19 Testing
Level: Laboratory Alert
After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.
Visit the FDA website for a list of authorized COVID-19 diagnostic methods. For a summary of the performance of FDA-authorized molecular methods with an FDA reference panel, visit this page.
In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test. CDC encourages laboratoriesto consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays can facilitate continued testing for both influenza and SARS-CoV-2 and can save both time and resources as we head into influenza season. Laboratories and testing sites should validate and verify their selected assay within their facility before beginning clinical testing.
Huawei is hiring Democratic lobbyist Tony Podesta as a consultant, according to two people familiar with the matter. Podesta will aim to help the controversial Chinese telecom giant warm relations with the Biden administration.
Politico