On December 24, the office will have reduced hours and be closed on December 25.
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Prior to vial assembly, vials are dry-heat sterilized and stoppers are steam-sterilized. The vials/stoppers are assembled on an automated line located in a Class 100 suite. The vials are subsequently capped in a Class 100,000 environment. Lot release sterility testing conforms to requirements set forth in USP <71>.