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Originally posted by Moshpet
We debunked this yesterday.
Move along.
www.abovetopsecret.com...
Mods this thread is a duplicate.
M.
A mock-up vaccine is a vaccine that mimics the future pandemic influenza vaccine in terms of its composition, manufacturing and control. However, instead of the pandemic influenza virus strain (which is unknown before the outbreak), the mock-up vaccine contains a strain of the influenza virus that has been specifically chosen because the population is immunologically naïve to it (i.e. has never been exposed to it).
After the final vaccine is ready, decisions on who should receive the vaccine, and when they should receive it, will be made by the government in each European Union Member State.
claims that the swine flu currently infecting the world was the result of genetic experiments by scientists which then leaked from a laboratory.
The extraordinary claims were made by 75-year-old Australian researcher Adrian Gibbs, who was part of the team behind development of the Tamiflu drug. Gibbs contends the deadly H1N1 strain may have been accidentally born in eggs scientists use to grow viruses and in vaccine research.
The objective behind a mock-up vaccine is to have a marketing authorisation (licence) in place, which can be changed quickly in the event of a pandemic to include the responsible virus strain, once it has been identified. The mock-up vaccine itself is not expected to be used or stockpiled (stored for use in the future) before the outbreak of a pandemic.
Once a pandemic has started, the company will first include the pandemic flu strain in the vaccine. It will then apply for a variation (a change to the vaccine’s marketing authorisation) by supplying full information to the CHMP on the vaccine including the new pandemic flu strain. Once the variation has been approved and been granted a marketing authorisation by the European Commission, the vaccine will be available for use. This variation will be processed quickly - normally within a few days - as most of the data on the pandemic flu vaccine will already have been reviewed during the assessment of the mock-up vaccine.
When will the pandemic vaccine be available?
Once the flu strain causing a pandemic is known, it takes about 12 weeks to prepare a suitable vaccine, as the viruses need to be grown in live cells, such as hens’ eggs.
After the final vaccine is ready, decisions on who should receive the vaccine, and when they should receive it, will be made by the government in each European Union Member State.
Also in Europe, some manufacturers have conducted advance studies using a so-called “mock-up” vaccine. Mock-up vaccines contain an active ingredient for an influenza virus that has not circulated recently in human populations and thus mimics the novelty of a pandemic virus. Such advance studies can greatly expedite regulatory approval.
hippocratic oath
Originally posted by Funshinez
"The population" in this context does not mean a human community, it means lab rats.
The EMEA’s scientific committee, the Committee for Medicinal Products for Human Use (CHMP), looks at data on the methods used to make and test the mock-up vaccine, as well as the results from studies of the vaccine tested in healthy people. This information covers the immunogenicity of the vaccine (its ability to make the immune system, the body’s defence mechanism, produce antibodies against the virus strain), as well as its safety (side effects).
Originally posted by wylekat
Keep in mind, the FDA is the one wanting to ban 'natural' stuff like herbs. However, they will unleash untested, dangerous 'vaccines' (which I dont even think IS a vaccine), make sure no legal recourse is available, and watch the stupid and ignorant swallow it without a second thought.
I love being an American.... NOT.