Susanne Posel, Contributor
The US government will assist the pharmaceutical corporations in finding prescription drugs to treat new diseases.
The focus of this collaboration will identify new uses for drugs that have already been approved by the Food and Drug Administration (FDA). There may be need for new human trials, putting the general public at a health risk. Engaging in experimental trials to classify specific compounds to be utilized for unintended purposes is highly dangerous.
Genetic engineering has led researchers to discover over 4,500 diseases that need pharmaceutical drugs to combat.
‘We need to speed the pace at which we are turning discoveries into better health outcomes,’ said Dr. Francis Collins, of the National Institutes of Health (NIH). ‘NIH looks forward to working with our partners in industry and academia to tackle an urgent need that is beyond the scope of any one organization or sector.’
The National Institutes of Health (NIH) will begin working with Pfizer Inc, AstraZeneca Plc and Eli Lilly and Co. in agreements to create compounds to be made available for trial use in a planned project.
‘Americans are eagerly awaiting the next generation of cures and treatments to help them live longer and healthier lives,’ Health and Human Services Secretary Kathleen Sebelius said in a statement. ‘To accelerate our nation’s therapeutic development process, it is essential that we forge strong, innovative, and strategic partnerships across government, academia, and industry.’
The pharmaceutical corporations are able to manipulate the FDA because the regulatory agency does not conduct independent studies on trial results. They simply accept the findings of the drug companies on their own trials.
Currently, the vitamin industries, by order of the Codex Alimentarius (CA) are being attacked by the US government to justify the force outlawing of natural medicine use.
The CA is a creation of the World Health Organization (WHO) and the Food and Agriculture Organization of the United Nations. The CA seeks to enforce international standards and codes on nations in a securitization of the world’s food supply.
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By controlling the means of food production, transportation and distribution, the CA will ensure the standards set forth by the UN are the basis for all national legislation.
Obama signed Executive Order (EO), Establishing the National Prevention, Health Promotion and Public Health Council in 2010.
Through this EO, Obama empowered the CA to enact the UN’s plan for worldwide food standards.
The National Prevention, Health Promotion, and Public Health Council was created to assist Obama in destroying the alternative health industry.
Congress fought the use of CA policy as the foundation for an attempt by the federal government to remove the American public’s ability to purchase vitamin supplements by deeming those remedies as “unscientific”. Since the FDA have consistently claimed that these alternatives have no medicinal value and decried their daily use a danger to a healthy lifestyle, social stigmas have served to aid Obama in declaring them useless. Obama suggests that their potency be changed to ultra-low levels in compound mixtures.
While the Obama administration seeks to wipe out the natural medicine industry, the US government is pouring money and resources into the genetic engineering of pharmaceuticals to combat disease.
When natural remedies are completely outlawed, the general public will be forced to take drugs rather than heal through diet and vitamins.
The medical agenda is clear.
The relationship between the US government and the drug corporations created by Obama has laid the foundation for medical tyranny.
Susanne Posel is the Chief Editor of Occupy Corporatism. Our alternative news site is dedicated to reporting the news as it actually happens; not as it is spun by the corporately funded mainstream media. You can find us on our Facebook page.