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USP 800

Learn more about standard USP 800

  • [White Paper] Workflow Strategies to Minimize Exposure to Hazardous Drugs in the Compounding Pharmacy

    [White Paper] Workflow Strategies to Minimize Exposure to Hazardous Drugs in the Compounding Pharmacy

    Handling hazardous drugs in the compounding pharmacy, per USP chapter <800> guidelines, involves strategic workflow strategies with the goal of minimizing personnel and environmental exposure.

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  • [Brochure] IV Workflow Compatible Primary Engineering Controls

    [Brochure] IV Workflow Compatible Primary Engineering Controls

    IV Workflow compatible primary engineering controls and containment primary engineering controls from NuAire maximize your pharmacy's production and safety.

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  • [White Paper] USP 800 Gap Analysis, A Business Perspective

    [White Paper] USP 800 Gap Analysis, A Business Perspective

    USP 800 is going to financially impact your pharmacy’s future business model so this white paper focuses on five important details that define the "why" for considering a capital investment.

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  • [White Paper] Can a Class I and Class II BSC be in the same Sterile Hazardous Drug (HD) Room?

    [White Paper] Can a Class I and Class II BSC be in the same Sterile Hazardous Drug (HD) Room?

    USP 800 does not directly address the pre-sterilization process of a sterile preparation creating the question can a class I and a Class II biosafety cabinet be used in the same sterile HD room?

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  • [Infographic] Flow Chart for USP 797 and USP 800 PEC Requirements

    [Infographic] Flow Chart for USP 797 and USP 800 PEC Requirements

    Navigate your primary engineering control options according to USP 797 and USP 800 with this flow chart.

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  • [White Paper] Facility and Engineering Controls Using USP 800 Guidelines

    [White Paper] Facility and Engineering Controls Using USP 800 Guidelines

    The focus of this article is to discuss the details for consideration of a good working design of a USP 800 compliant compounding lab.

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