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Monday, May 06, 2024 7:14:26 PM
What is needed.
DE- scheduling followed by full FDA approval. Then you can go uplist. Currently we have a decentralized, or perhaps fractioned environment, some states allow, some states don’t, some states with prescription. And all states have their own laws which don’t really align well.
When we get as far as the FDA, we will have new regulations, policies, procedures, potency limits, testing requirements and a hefty dose of quality controls in place that currently we don’t. Those will all be FED. controlled. Anyway, a simple explanation for a very complex issue.
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