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No serious adverse events
J., & Thachil, J
At present, regulatory agencies like the FDA and the European Commission evaluate CQDs on a case-by-case basis, irrespective of a specific regulatory procedure as these nanomaterials do not fit neatly within existing classifications for pharmaceuticals, biologics, or medical devices [172]
Even if the underlying problem is treated appropriately and the digestive tract returns to normal, the vomiting, diarrhea, and weight loss may continuebut now because of the vitamin B12 deficiency, not the initial disease process
That is why it is grouped with other research peptides rather than with approved medicines
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