At QX Ltd., we have written a software that uses the EPFX data in more avant garde ways. This software offers no risk and is completely safe. We recognize that this new type of system needs to be tested experimentally. The USA allows us to develop an Institutional Review Board and operate an Investigational Device Exemption for this software. To use this software in the USA we need to get informed consent from the patients or persons who are tested. Informed consent must be signed, implied, or understood.

The registered EPFX software and hardware uses a micro current medically safe pulse applied to the wrists, ankles and forehead. We safely measure some of the electrical aspects of the body. A variant micro current is then adapted to the patient to feedback the signal. The QXCI software will use the same medically safe standards to develop a wider range of variant wave forms to the body. The patient will choose and direct the therapy by their unconscious electrical reactions. The QXCI will also use a subspace system or Prayer wheel if there is no biological signals present. The system will show the patient reactions to homeopathic or nutritional items. This will help the therapist and the patient choose items that might be helpful. These choices are voluntary suggestions. The patient can greatly benefit from help with these choices. No items of significant risk are possible. These items are not part of the study and purchase of them is the patient’s responsibility.

There is insignificant risk and the only discomfort is sitting still for the 30 or 40 min evaluation. The patient name will be held confidential in the study. Participation is always purely voluntary. There is no penalty for withdraws. The other facts of the case are e-mailed to QX ltd IRB. The FDA of America reserves the right to inspect records. But confidentiality is always guaranteed.

The results of the studies are to be published on the International Journal of the Medical Science of Homeopathy. These results are available in 2006 on the internet or through your therapist. Over 35 studies on the device have already been published.

Since there are over 10,000 EPFX machines around the world, and all have access to the QXCI software, assuming 10 patient visits a week there might be over 400,000 data streams per month. We fully expect over a million bits of data in the first year alone. We will analyze all types of diseases - all types of clients - in one of the world’s largest studies of its kind. We welcome your participation.

The clinical therapist is responsible for ensuring that informed consent is obtained from each research subject before that subject participates in the research study. FDA does not require the therapist to personally conduct the consent interview. The therapist remains ultimately responsible, even when delegating the task of obtaining informed consent to another individual knowledgeable about the research.

The Centro Ricerche of Prof. William Nelson University of Venice + Padova, Italy Is the headquarters for the study IRB. There are researchers in over 25 different countries. If you have questions or comments please ask your therapist or send them in writing to www.irbqxci.net.

I am informed of the experiment on the QXCI software. I willingly give my consent to participate in the study. I give my consent for any children under my supervision or custody. I am to be guaranteed confidentiality of the data. I will be allowed to see the results of the publication in roughly one year. I recognize that there is no firm diagnosis resulting from the software. We are diagnosing and treating only Stress via Biofeedback.

I give my full and informed consent to partake in this research.

SIGNATURE________________________________________
DATE______________________________________________
THERAPIST OR WITNESS_____________________________
In short
1. The QXCI software research is to study millions of people with a wide variety of diseases to see who gets or feels better.
2. the QXCI software will allow the unconscious of the patient to guide to repair electrical and vibrational aberrations in your body.
3. The device and the study is always voluntary, confidential and safe.
4. There are a wide amount of benefits already displayed by the thousands of users and millions of patients. A millions of people have already been helped.
5. Results of the study and answers to your questions are available.