Health Care Reform Program
 SAFER DRUG APPROVAL & TESTING REFORMTPF believes that the entire drug approval process needs to be revised and “pulled back” in order to properly evaluate the new drugs introduced in the market. It is clear that due to the amount of “failed drug” recalls and class action suits, that Big Pharma is using patient’s input for additional “Testing” effects of manufactured drugs. It is clear that of all drugs being recalled and withdrawn from the market now, all were initially approved SAFE by the FDA under established criteria. The validity of FDA approval has been severely harmed by recent failures of the FDA to DO THEIR JOB! The policy and attitude of the AMA and FDA that “the dangers from side effects caused by most manufactured/engineered drugs are acceptable risks for treatment of disease and conditions” is NO LONGER ACCEPTABLE as in many cases the patient may remain asymptomatic and still experience ill side effects of drugs over long term while slowly causing accumulative injury or damage to the patient.
We support and work on behalf of all PACS that help further our cause in both the United states House and Senate along with rules and policies specific to the FDA and AMA. - Petition to protect open and unrestricted access to all natural supplements and remedy protocols that are under threat to be restricted by Special Interest Groups not interested in making medicine better for anyone.
- Petition for legislation to force more stringent FDA test policies, review processes, and “acceptability reqiurements” for medical processes and drugs.
- Petition for legislation to force drug companies to continue providing OLD drugs with now expired patents, to replace many of the new drugs that are synthetic and dangerous.
- Petition for legislation that requires FDA recommendation that all patients receiving anesthetics, chemo-therapy and/or radiation therapies be given IV Chelation therapy as a de-toxification therapy against toxins prescribed in these aforementioned therapies.
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