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Facility Management will be on hand to assist in any way possible.

Products manufactured as an aseptic parenteral have the greatest risk of contamination and must be manufactured in an area tolerating only the lowest level of risk.

Therefore, the greatest level of control over manufacturing must be proven.

It is the first set of enforceable sterile compounding standards issued by the United States Pharmacopeia (USP).

USP 797 describes the guidelines, procedures and compliance requirements for compounding sterile preparations and sets the standards that apply to all settings in which sterile preparations are compounded.