Application

Sterile Hazardous Drug Compounding

USP <800> Compliant Containment Primary Engineering Controls (C-PEC)

We specialize in Containment Primary Engineering Controls (C-PEC) for sterile compounding of hazardous drugs, meeting strict USP <800> standards. Our Class II, Type A2, and Type B2 Biosafety Cabinets (BSC) are designed to improve pharmacy workflow and simplify cleaning, ensuring safety and efficacy for healthcare professionals.

Restricted Access Barrier Systems (RABS), including the Compounding Aseptic Containment Isolator (CACI), provides alternative secure hazardous drug handling with integrated glove ports. This ensures the integrity of sterile preparations and safety of both products and personnel.

Sterile Hazardous Drug Compounding C-PEC

Application

Sterile Hazardous Drug Compounding

We specialize in Containment Primary Engineering Controls (C-PEC) for sterile compounding of hazardous drugs, meeting strict USP <800> standards. Our Class II, Type A2, and Type B2 Biosafety Cabinets (BSC) are designed to improve pharmacy workflow and simplify cleaning, ensuring safety and efficacy for healthcare professionals.

Restricted Access Barrier Systems (RABS), including the Compounding Aseptic Containment Isolator (CACI), provides alternative secure hazardous drug handling with integrated glove ports. This ensures the integrity of sterile preparations and safety of both products and personnel.

Our Hazardous Drug Compounding Equipment Benefits

NuAire’s sterile hazardous drug compounding equipment is designed not only to meet regulatory standards but also enhance the operational efficiency and safety in compounding pharmacy. Here’s how our equipment benefits healthcare professionals and pharmacy technicians.

Workflow and cleanability

Our containment primary engineering controls (C-PEC) are intuitively designed for workflow optimization, enabling pharmacists and technicians to work efficiently with fewer steps and less fatigue. The smooth, accessible surfaces simplify sterile environment maintenance, essential for safety and USP <800> compliance. The cleanability minimizes cross-contamination risks, improving overall pharmacy efficiency.

Ergonomics

Ergonomic design is central to our equipment development, prioritizing the physical comfort of pharmacy staff in high-pressure settings. Our biosafety cabinets and isolators feature adjustable heights and ample space, minimizing strain, reducing repetitive stress injuries, and improving focus on precise compounding tasks.

Dependability

Reliability is essential in hazardous drug compounding, and our equipment is designed for consistent performance. Built with durable, high-quality materials, our products ensure long-term dependability, minimizing downtime and maintaining steady production in high-demand pharmacy settings.

Innovative technology

We utilize cutting-edge cleanroom and containment processes to provide top-tier solutions for handling hazardous drugs. Advanced air filtration, secure barrier technologies, and automated systems ensure safe handling, protecting both the work environment and the purity of medications, which directly impacts patient safety.

Patient care and safety

Advanced compounding equipment improves patient safety by ensuring medications are prepared in a precise, controlled environment. This reduces contamination and dosing errors, resulting in better health outcomes. Enhanced workflow efficiency also allows pharmacy staff to focus more on patient care, improving overall service delivery and patient satisfaction.

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Related Resources

Infographic

10 Tips for Working Safely in the Pharmacy with Your Biosafety Cabinet

The Infographic provides ten tips for working safely in a drug-compounding pharmacy with a Biosafety Cabinet (BSC).
Infographic

USP 797 and USP 800 PEC Requirements

Follow this flowchart for an easy method to identify what Primary Engineering Control (PEC) or Containment Primary Engineering Control (C-PEC) your pharmacy needs.
White Paper

USP 800 Gap Analysis

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.
White Paper

Facility and Engineering Control Design Under USP 800

Design considerations for creating a Pharmacy USP 800 compliant Hazardous Drug (HD) compounding operation.
White Paper

Creating a USP 800 Compliant Cleanroom

A well-designed hazardous drug (HD) cleanroom must account for a variety of factors to ensure USP 800 compliance.
Webinar

Cleanroom Certification for USP 800

From PPPmag watch and list to Jim Wagner, President of Controlled Environment Consulting, speak on cleanroom certification for USP 800.
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Cleanroom Layout Design Under USP 800

Learn the necessary elements to establish a cleanroom layout under USP 800.
Webinar

Cleanroom Design Under USP 800 Preparing for Construction

Listen to Jim Wagner, President of Controlled Environment Consulting, discuss how to construction considerations before your USP 800 cleanroom installation.
White Paper

How to Perform a Hazardous Drug Risk Assessment in the Compounding Pharmacy

How to Perform a Hazardous Drug Risk Assessment in the Compounding Pharmacy.
Webinar

USP Compliance PEC Cleaning and Decontamination

Fred Massoomi outlines how to establish standard operating procedures (SOPs) for cleaning PECs, the level of detail required for these SOPs, and staff training requirements.
White Paper

Environmental Sampling Guidance in the Pharmacy

Discover best practices for environmental monitoring in pharmacies with our white paper, "Environmental Sampling Guidance in the Pharmacy." Get insights into equipment selection, results interpretation, and future trends in rapid testing methods.
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