Leveraging IV compounding automation to streamline cleanroom processes can help improve operational efficiency and enhance patient safety, while maintaining compliance with USP <797> Beyond-Use Dates.

By leveraging the clear advantages of automation and embracing USP 797 as an opportunity to advance competency and accountability within its pharmacy department, Sentara RMH has laid a foundation ...

The USP 797 Clean Room allows for all types of complex extemporaneous compounding for low, medium and high risk investigational compounds. This allows ...

ENGLEWOOD, Colo., Nov. 14 Baxa Corporation announces plansto bring together industry thought leaders for a day-long forum on cleanroomcompliance and best practice. Active members from the United ...

WALTHAM, Mass., December 09, 2024--Wolters Kluwer Health integrates data from Sonicu continuous environmental monitoring platform into Simplifi 797 USP compounding compliance solution.

On January 1, 2004, chapter 797 of the United States Pharmacopeia (USP) became the nation's first enforceable standard for the compounding of sterile preparations. [1,2] This new standard was ...

Penguin Innovations’ virtually interactive cleanroom reflects a realistic pharmacy environment. The virtual cleanroom is the only one of its kind that adheres to United States Pharmacopeia USP <797> ...

WEST LAFAYETTE, Ind., and INDIANAPOLIS – A Purdue-related startup is developing the first USP 797 certified, virtual pharmacy cleanroom laboratory for students and other industry professionals to gain ...

MINNEAPOLIS--(BUSINESS WIRE)-- DaVita Clinical Research® (DCR®), a provider of clinical research services focused on kidney research as well as a multitude of specialty therapeutic populations, ...

The rigor of USP chapter 797 exceeds what is necessary for hospital pharmacy practice (n = 250) 3.86 (3.69 4.03) a USP = United States Pharmacopeia , CI = confidence interval.