Our pharmacy network follows USP <797>, the standard that governs the strength, quality, and purity of compounded sterile preparations. Under this standard, every batch is tested to confirm the active ingredient falls within 90 to 100% of its labeled concentration.
Sterile products are also tested for sterility and endotoxins before they can ship, as required under that same standard. 503(a) pharmacies are licensed and inspected by their state board of pharmacy, and 503(b) outsourcing facilities register with the FDA and follow current Good Manufacturing Practice (cGMP) requirements, the same category of oversight traditional drug manufacturers are held to.