FDA IS NOT A SCIENTIFIC BODY
AND CANNOT MAKE SCIENTIFIC JUDGEMENTS, PARTICULARLY ON SUBJECTS THAT IT HAS NO JURISDICTION, WHICH ARE NOT FOOD OR DRUGS, BUT FOR SOMETHING THAT IS BEYOND FDA, SUCH AS MECHANICAL DEVICES.
IS FDA A SECRET AGENCY ITSELF AGAINST HUMANITY ?
FOR SECRET SOCIETES CLIK HERE
www.papimi.gr/sam.htm
with explanatory notes
FOR DETAILS ON BOOKS ON FDA CLICK HERE
www.papimi.gr/fb.htm
self explained
ATTENTION: PRESIDENT OBAMA
FOR DETAIL PROOFS OF THE CLAIMS BELOW, SEE PREVIOUS SELECTION IN THE SELECTION COLUMNThe three false incidents FDA and Michael Berens refers to, for
PAPIMI, they never happened then, they were never happened before, and they were never repeated afterwards,
world wide. Papimi is the same device in all these years, for about 20 years
Papimi has been approved as a safe medical device in the most parts of the
world, saving and helping millions of people, including its operation in USA for
thousands of American people now, together with some 10 different brands and
under-performing illegal copy papimi devices in USA
We obviously would like to ask, Is FDA promoting the copy
papimi devices, like this, in USA and in the rest of the world ?
Is this the way, USA achieves its technology each time ?
We can say with proud, that PAPIMI is in one of the safest device known today, with no real side effects known, in the service of humanity and its people. Different claims compete this humanitarian function for reasons better known to those "competitors" themselves .
Pappas is only the patent author of the PAPIMI device. He is not the manufacturer, he is not a distributor, he is not the representative of any kind. He has nothing to do with the Investigational Review Board that the FDA refers above. He does not know any of the clinical studies, their location or what they are doing.
However FDA is asking Pappas as above to interfere in the above investigation, ignoring their own rules and laws of USA and FDA acting as a ''Peasant first time coming to a Big City'' or as a ''Gangster first time coming to a Big City''.
SEE RELEVANT LETTER OF TABS BELOW
THE TRUTH IS:
PAPIMI DEVICE IN ALL LAST 20 YEARS HAS PROVEN THAT
PAPIMI IS A NON SIGNIFICANT RISK DEVICE
WITH NONE ADVERSE OR SIDE EFFECT TODAY, SEPTEMBER 2009.
PAPIMI IS PRODUCING A NON RADIATIVE MAGNETIC FIELD.
MOST 0F THE ENERGY >99.9%FOR EVERY MAGNETIC PULSE IS SPENT FOR ESTABLISHING THE NECESSARY ELECTRICAL CURRENTS THROUGH ITS MAGNETIC COIL.
FDA IS CLAIMING NONSENSE WRITING THAT ABOUT 100 WATTS PER
PULSE IS DELIVERED TO A SUBJECT EXPOSED TO PAPIMI.
UNQUESTIONABLE INDEPENDENT PROOF OF THIS IS THE FACT THAT EXPOSING
UNLIMITED HUMAN EYES IN CONTACT WITH THE COIL, PROVIDED THE COIL IS NOT HEATED
OR HOT, NO EXCESS
HEATING TO THE EYES RESULTS OR ANY OTHER ADVERSE EFFECT
ON THE CONTRARY VISION IS FOUND TO INCREASE CONSIDERABLY AND PARTICULARLY IT IS FOUND TO INCREASE NIGHT VISION AND TO DECREASE PRESBIOPIA WHICH USUALLY OCCURS WITH AGING.
TTHE ABOVE DOCUMENT OF FDA- FOOD AND DRUG ADMINISTRATION IS
ILLEGAL, POLITICAL AND NON SCIENTIFIC.
(for verification, click here)
FDA AS AN ADMINISTRATIVE BODY HAS NO AUTHORITY TO MAKE SCIENTIFIC JUDGEMENTS.
ALL PAPIMI CLINICAL STUDIES (INITIALLY ABOUT 200) WERE RUNNING LEGALLY UNDER THE RESPONSIBILITY OF THE INVESTIGATIONAL REVIEW BOARD-IRB, TABS OF TEXAS.
THE ABOVE LETTER WAS WRONGLY ADDRESED TO PAPPAS.
FDA'S CRIMINAL GOAL......
SCIENTIFIC SUPPRESSION OF VERY EFFECTIVE AND ECONOMICAL METHODS.
SEE ALSO :
THE CRIME OF PROHIBITING SAVING www.papimi.gr/suppresion1.htm
The unbelievable adventures of the SUPPRESSED Miraculously Effective and Innocuous Alpha-Stim Device, favorably mentioned worldwide, possessing all Medical Approvals and Licenses and sold freely in Europe, while in USA is being unjustifiably classified as a Class III "Significant Risk Device", requiring Doctors prescription... www.papimi.gr/politics.htm
ELECTROMEDICINE : THE OLDEST, MOST EFFECTIVE, MOST SUPPRESSED MEDICAL THERAPEUTIC TECHNOLOGY www.papimi.gr/ELECTROMEDICINE.htm
The SUPPRESSED Priore Electrotherapeutic Device is a scandal in the Politics of Science : www.rexresearch.com/priore/priore.htm www.cheniere.org/priore/index.html www.cheniere.org/books/aids/appendixI.htm
The SUPPRESSED Lakhovsky Electrotherapeutic Device : www.rexresearch.com/lakhov/lakhusps.htm www.papimi.gr/lakhovsky.htm
The SUPPRESSED Dotto Electrotherapeutic Device : www.rexresearch.com/dotto/dotto.htm
Dr. Margaret (Meg) Patterson, a SUPPRESSED Pioneer in Electromedicine, had to battle the hostility and suspicion that previously marked her peers attitudes against Neuroelectric Therapy (NET), her significant contribution to the treatment of addiction. www.papimi.gr/patterson.htm
"....Why does a U.S. cancer patient, with a localized tumor, have to travel outside the U.S. to receive EChT treatment? Why EChT is SUPPRESSED and it is not available in the U.S.? " http://www.iabc.readywebsites.com/page/page/623958.htm
INDEED THE ABOVE LETTER OF FDA SIGNED BY ONE PERSON- MARCARELLI OBVIOUSLY SCARED IR BOARD OF TABS BY ITS LETTERHEAD OF FDA. TABS UNDERSTIMATED ITS AUTHORIRITY AGAINST ITS MASTER FDA AND MARCARELLI, AND DECIDED UNQUESTIONABLY EVEN MORE... TO HALT ALL THE CLINICAL STUDIES IN EXISTENCE, INSTEAD OF CONTINUING THEM, AS MARCARELLI HIMSELF WAS ASKING. OBVIOUSLY TABS THOUGHT THIS WAY THAT ITS MASTER WILL BE MORE PLEASED.
THIS WAY, FDA WITH ITS FALSE CLAIMS, CAUSED ONE MORE TIME THE PROCEDURE FOR APPROVAL OF PAPIMI TO BE HALTED. THE SAME TIME FDA MANAGED TO AVOID MAKING PUBLIC TO SCIENCE THE PAPIMI'S UNAMBIGUOUS EXCELLENT RESULTS. Click here to read about the previous times of applications for approval of PAPIMI in USA
NEVERTHELESS, PAPIMI IS APPROVED AND ENJOYED IN ALL THE REST OF THE WORLD, AS A SAFE MEDICAL DEVICE FOR USE ON HUMAN SUBJECTS, WITH EXCEPTION OF USA, JUST BECAUSE OF THE CRIMINAL ACTIONS OF USA FDA.
Who owns the FDA ? The drug industry or the people ?
From the book "OVERDO$ED AMERICA : The broken promise of American Medicine" by John Abramson
"The FDA has fallen under the influence of the drug and medical device industries so much, so that it was labeled "a servant of industry" by Dr. Richard Horton, the editor of the British journal The Lancet.
=========================================================================================
=========================================================================================
