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The decision point is financial
What "Research Use Only" Actually Means "Research use only" is a regulatory and labeling designation, not a marketing description
39 For these high-risk candidates, the 503B should pre-emptively establish relationships with API suppliers, develop and validate compounding and testing protocols, and prepare the necessary documentation
The FDA approval process means these medications have been studied in large clinical trial populations, their manufacturing facilities are inspected by the FDA, and their labeling (including dosing instructions, warnings, and side effects) has been reviewed and approved by federal regulators
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There can also be a risk of worsening eye problems related to diabetes, like diabetic retinopathy and problems with the central part of the retina (macula)
