In my research this morning, I think I may have found where the e-cigs fit. My suggestion is that we look into the rules and regulations of becoming a Homeopathic or Allopathic drug.
Why? The Homeopathic drugs are submitted to HPCUS. Now, with NicoWater, they were given trouble by the FDA and reforumulated their nicotine concentration to be below 4 mg per dose which drops them into the homeopathic category. We have calculated our dosage lists based on the manufacturers info and the High Nicotine carts fall under 4 mg per dose... actually well under. And technically, as the no nicotine has no nicotine, it doesn't need to be regulated at all.
With homeopathic drugs, you present to HPCUS as you would to the FDA, but you need two clinical trials and samples. (Of which we will be able to provide with the Auckland study and Dr. Lio?) The process is shorter and faster.
Allopathic drugs go through the FDA, but are not held to the same restrictive process as an NRT/NDP.
I thought I would put this out there so others could help me on my lead. We all talk of where does the e-cig fit. Either way, we DO NOT want to be lumped into the NRT/NDP category. Here is a link to the HPCUS website for anyone who is interested. Register | Login | Edit Acco
Here is another interesting note: FDA doesn't have control of tobacco, however, their formula looks kind of like this - "Device" = tobacco = nicotine-delivery device but tobacco does not = class of device. Yep... that's the FDA for you.
Why? The Homeopathic drugs are submitted to HPCUS. Now, with NicoWater, they were given trouble by the FDA and reforumulated their nicotine concentration to be below 4 mg per dose which drops them into the homeopathic category. We have calculated our dosage lists based on the manufacturers info and the High Nicotine carts fall under 4 mg per dose... actually well under. And technically, as the no nicotine has no nicotine, it doesn't need to be regulated at all.
With homeopathic drugs, you present to HPCUS as you would to the FDA, but you need two clinical trials and samples. (Of which we will be able to provide with the Auckland study and Dr. Lio?) The process is shorter and faster.
Allopathic drugs go through the FDA, but are not held to the same restrictive process as an NRT/NDP.
I thought I would put this out there so others could help me on my lead. We all talk of where does the e-cig fit. Either way, we DO NOT want to be lumped into the NRT/NDP category. Here is a link to the HPCUS website for anyone who is interested. Register | Login | Edit Acco
Here is another interesting note: FDA doesn't have control of tobacco, however, their formula looks kind of like this - "Device" = tobacco = nicotine-delivery device but tobacco does not = class of device. Yep... that's the FDA for you.