~ George Washington
The Food and Drug Administration's responsibility is to protect the public interest. Their charge is to ensure the safety and reliability of industry claims before issuing approval for public consumption. Our doctors rely on the FDA's safety standards to make important decisions about our individual care. Policymakers use this same information to make broad decisions that impact us all. But what happens when they're wrong? What is the impact of the FDA's deficiencies? Pharmaceutical products and other consumable goods are brought to market that can be dangerous; causing injury, suffering, and even death. Industry giants are permitted to conduct their own safety studies without objective third-parties and as a result of this severely lacking oversight, many have been found guilty of criminal fraud, illegal kickbacks, and failure to report safety data. More regulation won't solve the problem; education and transparency will.
Transparency can be achieved through fair and balanced reporting. The problem is that Direct to Consumer Marketing allows industry giants to control the media narrative. An estimated 70% of all sponsorship dollars to every major news network come from pharmaceutical companies. This creates a clear conflict and sure barrier to balanced, honest reporting. Direct to Consumer Marketing compromises free press. Credible voices are silenced and all too often, by the time dangers are reported, the damage has already been done. Add your name to the petition and help remove the barriers of a truly free press. Together, we can achieve the transparency we deserve.
Bias in the Media is slanted toward industry giants. Researchers warned of the dangers of glyphosate for at least a decade before it made the headlines.
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~ Thomas Jefferson