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(NaturalNews) A
group of scientists working in the FDA’s Center for Devices and Radiological
Health division has revolted against the corrupt managers of its own department,
accusing them of committing crimes by claiming, "There is extensive documentary
evidence that managers at CDRH have corrupted and interfered with the scientific
review of medical devices."
Read the letter yourself here (PDF):
http://energycommerce.house.gov/Press_110/110-ltr-101408.CDRHscientists.pdf
The
letter from the FDA's own scientists goes on to say, "It is evident that
managers at CDRH have deviated from FDA's mission to identify and address
underlying problems with medical devices before they cause irreparable harm, and
this deviation has placed the American people at risk."
Congressman John,
Dingell, chair of the committee which received the letter, went on to charge
that these FDA bureaucrats "approved or cleared medical device applications in
gross violation of laws and regulations..." (http://energycommerce.house.gov/Press_110/110nr383.shtml)
None
of this, of course, surprises readers of NaturalNews. Note, too, that the
mainstream media has virtually ignored this story? You might think that a revolt
of FDA scientists against their criminal bosses would be a huge story worthy of
front-page treatment at USA Today or the Washington Post, right? Only the NY
Times bothered to report this story, as far as I can tell. (http://www.nytimes.com/2008/11/18/health/policy/18fda.html)
The FDA: A gang of unindicted criminals
The FDA, you see, is a criminal
organization engaged in tactics of intimidation, censorship and oppression that
can only be properly called "terrorism." Don't take my word for it, though: The
FDA's own top scientists are now on the record saying much the same thing! Their
complaint to Congress alleges top FDA managers "ordered, intimidated and coerced
FDA experts to modify their scientific reviews, conclusions and recommendations
in violation of the law.”
Keep in mind this is from the FDA's own
scientists! This isn't some outsider (like me) ranting about the FDA being a
criminal organization; these are the words of the very people who work
there!
Even the FDA director is like an evil character out of a Marvel
comic. His name is actually Dr. von Doom... er, I mean Dr. von Eschenbach, and
he has routinely ignored the multiple letters sent to him by these scientists
complaining of the same criminal behavior taking place at the agency.
The
FDA, of course, believes it is above the law and subject to no rules whatsoever.
It is a political organization, and a criminal one at that. It will likely
threaten these scientists just as it once threatened Dr. David Graham, and it
will use every intimidation tactic at its disposal to discredit any employee who
dares challenge the power and authority of the FDA.
I wouldn't be
surprised one day to find one of these intimidated scientists showing up at work
and going Columbine on a few of the top FDA officials who are the masterminds
behind these crimes against humanity. If that happens, perhaps the saying,
"Going Postal" will be updated as, "Going FDA."
Because if there's anyone
with a justified reason to be violently angry at their bosses, it's gotta be
this group of intimidated scientists who are trying to save people's lives by
making FDA approvals based on solid science. Instead, they're being routinely
overruled by politics and Big Pharma deception, which they know will result in
the loss of human life as consumers are harmed or killed by dangerous medical
devices and pharmaceuticals.
How would you like to work at a company with
a crime boss, knowing your boss is a white-collar criminal whose decisions are
going to get people killed? That's the reality these FDA scientists live with
every day! And they're tired of it. They're beginning to revolt...
Violence will not solve this problem
Here's a question to you: When the
FDA collapses, should the top managers be tried for their crimes, or simply
hanged by their necks in the streets? Since I believe in non-violent solutions
to such problems, I believe we should actually grant them all amnesty in
exchange for their candid testimony before Congress, where they spill their guts
about all the criminal acts they've engaged in over the years.
Their
testimony will be a lot more valuable to society than a bunch of bodies swinging
from the rafters. What we need here, folks, is to learn the lessons from
this rogue agency, not to take revenge on its people.
Not everybody
agrees with me on this. But I repeat to everyone listening: Do NOT engage in
violent acts against the FDA, even if there is some social breakdown in the
future that might give you such an opportunity. More than 90% of the people who
work there are honest, hardworking individuals who are trying to fight the FDA's
crimes from the inside. We need to let law and order sort out the criminals from
the good guys, and then we'll work together to demand criminal sentencing for
them, which I think should include ex-FDA bureaucrats going door to door selling
Girl Scout Cookies to raise money to pay back the families of all the people
killed by FDA-approved drugs.
Remember: The medical violence that the FDA
now directs towards the public should NOT be met with vengeful violence on the
part of activists. It should be met with justice and wisdom for future
generations. A little compassion can help us move past this dark era of FDA
dominance and into a new golden age of true healing. But we cannot get to an era
of healing if our own actions are motivated by violent acts.
Violence is
the tool of the weak. That's why the FDA uses the threat of violence to raid
vitamin companies. Healing is the tool of the strong.
If we hope to move
beyond the treacherous philosophies the FDA is demonstrating today, we must
transcend violence and rely on healing (at many levels) to move us past
this dark era.
The big question right now, of course, is: When will the
FDA arrests begin? January 21st might be a good day to get that
started...
Sources:
Letter from FDA scientists:
http://energycommerce.house.gov/Press_110/110-ltr-101408.CDRHscientists.pdf
Statement
of Congressman John Dingell:
http://energycommerce.house.gov/Press_110/110nr383.shtml
(Full
copy included below)
Pharmalot article, the original source for this
story:
http://www.pharmalot.com/2008/11/congress-probes-corrupted-fda-device-approvals/
Congressman John Dingell's statement:
Dingell, Stupak to Investigate
FDA’s Medical Device Approval Process
Lawmakers Question Whether
FDA Knowingly Allowed Unsafe & Ineffective Medical Devices into U.S.
Market
Washington, D.C. - Reps. John D. Dingell (D-MI), Chairman of
the Committee on Energy and Commerce, and Bart Stupak (D-MI), Chairman of the
Subcommittee on Oversight and Investigations, today launched an investigation
into whether managers within the Food and Drug Administration (FDA) Center for
Devices and Radiological Health (CDRH) knowingly corrupted the scientific review
process and approved or cleared medical device applications in gross violation
of laws and regulations designed to assure the safety and effectiveness of
medical devices. Such activity could allow potentially unsafe and ineffective
medical devices into the U.S. market.
The investigation was prompted by
receipt of an October 14, 2008, letter written on behalf of a large group of
CDRH scientists and physicians who state that CDRH managers have “corrupted and
interfered with the scientific review of medical devices.”
“These
allegations are deeply concerning, and we intend to uncover whether any FDA
activity has compromised the health and safety of America consumers,” said
Dingell. “I commend the FDA scientists for courageously sounding the alarm on
what appears to be a serious problem. I look forward to pursuing the steps
necessary to ensure that the medical devices Americans depend on are safe and
effective.”
“Our investigations have found that the FDA has allowed
contaminated food and unsafe drugs to enter the market, and now serious
allegations have been raised about the scientific integrity of the FDA medical
device approval process,” Stupak said. “Although the FDA has launched its own
investigation into this matter, no corrective action has been taken. The
committee intends to learn what action the FDA plans to take to ensure the
integrity of the medical device approval process and prevent retaliation against
the scientists who blew the whistle on these activities.”
This Committee
has been provided with compelling evidence to support the charges that senior
managers within CDRH “ordered, intimidated and coerced FDA experts to modify
their scientific reviews, conclusions and recommendations in violation of the
law.” The CDRH scientists also claim that CDRH managers ordered them “to make
safety and effectiveness determinations that are not in accordance with
scientific regulatory requirements, to use unsound evaluation methods, and
accept clinical and technical data that is not scientifically valid or obtained
in accordance with legal requirements, such as obtaining proper informed consent
from human subjects.”
Additionally, documentary evidence reviewed by this
Committee indicates that CDRH scientists who raised concerns up their chain of
command have experienced reprisals for their insistence on adherence to a
scientific and regulatory basis for medical device review. To protect these CDRH
scientists who have risked their careers to bring their concerns to the
attention of this Committee, we will not disclose their identities at this
time.
Since January 2007, the Committee on Energy and Commerce and its
Subcommittee on Oversight and Investigations have been investigating the ability
and commitment of the Food and Drug Administration to protect Americans from
unsafe food, drugs, and medical devices. For more information about the
Committee’s ongoing drug safety investigation visit:
http://energycommerce.house.gov/Investigations/FDADrugSafety.shtml
During
this Congressional session, Committee leaders released draft legislation aimed
at improving the safety of food, drugs, devices, and cosmetics. Work in this
draft bill, the “Food and Drug Administration Globalization Act," continues.
Committee leaders plan to introduce comprehensive legislation early next
session. For more information visit: http://energycommerce.house.gov/FDAGlobalAct-08/index.shtml
In
a letter sent today to FDA Commissioner Andrew C. von Eschenbach, Dingell and
Stupak requested a briefing on what actions the Commissioner has taken to date
and how the Commissioner intends to resolve all issues raised by the CDRH
scientists and physicians.
About the author: Mike Adams is a
consumer health advocate with a mission to teach personal and planetary health
to the public He has authored and published thousands of articles, interviews,
consumers guides, and books on topics like health and the environment, impacting
the lives of millions of readers around the world who are experiencing
phenomenal health benefits from reading his articles. Adams is a trusted,
independent journalist who receives no money or promotional fees whatsoever to
write about other companies' products. In 2007, Adams launched EcoLEDs, a maker
of energy efficient LED lights that
greatly reduce CO2 emissions. He's also a noted pioneer in the email marketing
software industry, having been the first to launch an HTML email newsletter technology that
has grown to become a standard in the industry. Adams volunteers his time to
serve as the executive director of the Consumer Wellness Center, a 501(c)3
non-profit organization, and enjoys outdoor activities, nature photography,
Pilates and adult gymnastics. Known on the 'net as 'the Health Ranger,' Adams
shares his ethics, mission statements and personal health statistics at http://www.healthranger.org/
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