‘Mock-Up’ Vaccines

[gramma lois]

EXCERPT: WHO Admits to Releasing Pandemic Virus into Population via ‘Mock-Up’ Vaccines

 

Dr. Mercola

Mercola.com

September 5, 2009

 

"The document on the WHO website linked below states that it is common procedure to release pandemic viruses into the population in order to get a jump ahead of the real pandemic, so as to fast track the vaccine for when it is needed.

 

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.

 

According to the website, “Such advance studies can greatly expedite regulatory approval.”

 

Sources: World Health Organization

 

Dr. Mercola’s Comments:

 

On June 11 the World Health Organization (WHO) raised its swine flu pandemic alert from a 5 to a 6. Phase 6 is the highest level alert, and reflects the speed with which a virus is spreading — not its severity.

 

This classification also allows for a vaccine to qualify for a “fast-track” procedure for licensing and approval, and this process is now ongoing for the swine flu vaccine.

 

What you may not know, however, is that WHO, together with health officials, regulatory authorities and vaccine manufacturers, have been working since 2007 – long before this new “threat” of swine flu emerged – to “explore a broad range of issues surrounding the regulatory approval of pandemic vaccines.”

 

According to the WHO website:

 

“Ways were sought to shorten the time between the emergence of a pandemic virus and the availability of safe and effective vaccines.”

 

Rest of Article Here:

http://articles.mercola.com/sites/articles...p-Vaccines.aspx

[Homemaker]

No surprise for me. They'll stop at nothing to manipulate us all into doing what they want. There's big money in creating a crisis and then selling us the "solution."

[Violet]

So, you are saying this is a farce ? What about the boy that just died ?

[Homemaker]

I'm not saying the virus is not real, neither is Dr. Mercola's article. I'm just agreeing with the WHO's admission that they release virus' into the population in order to generate a crisis that gets vacines approved without the lengthy safety tests. The quicker they can get people buying their latest vaccine, the quicker they can get rich off it.

[gramma lois]

I'm not saying the virus is not real, neither is Dr. Mercola's article. I'm just agreeing with the WHO's admission that they release virus' into the population in order to generate a crisis that gets vacines approved without the lengthy safety tests. The quicker they can get people buying their latest vaccine, the quicker they can get rich off it.

 

Excerpt from WHO Website

 

*Link http://www.who.int/csr/disease/swineflu/no...5/en/index.html

 

 

"Pandemic (H1N1) 2009 briefing note 6

 

6 AUGUST 2009 | GENEVA -- WHO

 

Pandemic influenza vaccine manufacturing process and timeline

6 August 2009

 

In 2007, as part of preparedness for an influenza pandemic, WHO worked together with health officials, regulatory authorities, and vaccine manufacturers to explore a broad range of issues surrounding the regulatory approval of pandemic vaccines. [1]

 

Ways were sought to shorten the time between the emergence of a pandemic virus and the availability of safe and effective vaccines. Different regulatory pathways were assessed, and precautions needed to ensure quality, safety, and effectiveness were set out in detail.

 

 

Fast-track procedures for approval

 

Regulatory authorities have shown great flexibility in developing procedures for fast-tracking the approval and licensing of pandemic vaccines.

 

In some cases, pandemic vaccines are not regarded by regulatory authorities as entirely “new” vaccines, as they build on the technology used to produce vaccines for seasonal influenza, established procedures for testing and regulatory control, and an extensive body of safety data.

 

In such cases, approval procedures are similar to those applied to “strain changes” made each year when seasonal vaccines are modified to match circulating viruses in the Northern and Southern Hemispheres.

 

Specific regulatory procedures have been devised to expedite the approval of pandemic vaccines. In the USA, for example, fewer data are required when the manufacturer already has a licensed influenza vaccine and intends to use the same manufacturing process for its pandemic vaccine.

 

In the European Union, the European Medicines Agency uses a rolling review procedure whereby manufacturers can submit sets of data for regulatory review as they become available, without having to wait until all data can be submitted together in a single formal application.

 

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."

 

 

Gramma Lois Notes: The purpose of posting (and gleaning) information is so that informed decisions can be made regarding whether or not to choose to receive this vaccine. I for one choose not to get it, however some may choose (did I say choose?) to get it, unless that is they have no choice in the matter if mandatory innoculations are the order of the day.

 

To each his/her own and may God bless you in your choices.