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Specifically, the panel will assess whether those substances should be moved off the Category 2 list a designation reserved for bulk drug substances that present potential safety risks and are therefore ineligible for routine compounding under Section 503A of the Federal Food, Drug, and Cosmetic Act

Nevertheless, a risk is present

Appropriate laboratory monitoring should be individualized according to the peptide prescribed, the patient's medical history, and current clinical practice guidelines, so what gets tested will not look identical for every compound

Proper methods of peptide storage and prep call for bacteriostatic water , sterile vials, insulin syringes, and other lab essentials