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This makes it particularly useful when working with compounds that require precise dilution or repeated preparation

Under a 1997 law, the first passed by Congress to regulate the industry, compounders can only use ingredients that are a component of an approved drug, have whats known as a USP monograph (essentially a third-party certified recipe for a drug used mainly by manufacturers of generics), or are listed as approved substances by the FDA

We hope this gives some insight into the problematic nature of pinpointing cause and effect within the constraints of such a complex environment

Once a gray market is thriving, who, if anyone, will foot the bill for rigorous research