The Smarthood is a fully integrated primary engineering control (PEC) that consolidates the entire IV compounding workflow into a single hood. Traditional IV preparation requires technicians to move between separate devices for scanning, documentation, weight verification, and labeling, each transition introducing potential for error and lost time. By bringing all of these steps together inside the sterile field, the Smarthood reduces physical movement, minimizes workflow interruptions, and supports cleaner documentation from start to finish.

Both Smarthood configurations come fully equipped with integrated barcode scanning, photo capture, a field of view camera, a built-in PC, Jabra speakers for enhanced communication, sterile label printing, and easy integration with existing IV workflow software. Scanning confirms correct drug and diluent selection, photo capture and the field of view camera create a comprehensive visual record of each compound, and the built-in label printer produces sterile labels without any external equipment. Gravimetric verification is available for both models as an optional upgrade, providing real-time weight-based accuracy checks for facilities that want an additional layer of compounding precision.

Yes. The Smarthood is available in two configurations, one for hazardous drug compounding (BSC Model) and one for non-hazardous compounding (Laminar Flow Hood Model. The Smarthood’s are built to meet the requirements of USP <797>, which governs sterile compounding practices, and USP <800>, which sets the standards for the safe handling of hazardous drugs in pharmacy settings. Whether your team is preparing standard sterile preparations or working with hazardous agents, the Smarthood provides a compliant, purpose-built environment that supports both safety and efficiency.

Compounding errors most often occur at transition points, when technicians step out of the sterile field, move between devices, manually transcribe information, or work around gaps in the verification process. The Smarthood eliminates those vulnerabilities by keeping the entire workflow within a single controlled environment. Real-time gravimetric verification confirms accuracy at every step, and integrated image documentation creates an automatic audit trail, helping teams catch errors before any preparation reaches the patient.

A horizontal laminar flow hood is a clean air workstation used in sterile compounding environments to protect products and materials from airborne contamination. It works by pulling room air through a pre-filter and then through a HEPA filter, which removes 99.99% of particles and organisms 0.3 microns or larger, before releasing the purified air as a continuous stream of positive pressure, unidirectional airflow that flows horizontally from the rear of the unit toward the operator. The HEPA filter is positioned at the back of the work area and protected by a removable perforated stainless steel diffuser, ensuring the work surface is continuously bathed in ISO 5/Class 100 clean air with minimal turbulence. Because the airflow moves toward the user rather than away from them, horizontal laminar flow hoods are designed exclusively for non-hazardous sterile compounding. Horizontal Laminar Flow Hood’s protect the product, not the operator.

The primary difference between a horizontal and vertical laminar flow hood is the direction of HEPA-filtered airflow across the work surface. In a horizontal hood, air flows from the rear of the unit forward toward the operator, while in a vertical hood, air is discharged from the top and flows downward toward the work surface before being drawn into return vents. Both configurations maintain ISO Class 5 conditions within the work zone, but horizontal hoods tend to offer more consistent airflow uniformity and are less susceptible to disruption from the operator’s hand and arm movements during compounding. The right choice depends on your specific workflow, the drugs being compounded, and your facility’s regulatory requirements.

USP <797> establishes standards for the preparation of all compounded sterile preparations, covering environmental quality, beyond-use dating, personnel training, and contamination control to ensure patient safety. USP <800> focuses specifically on the safe handling of hazardous drugs across the entire drug-use process, from receipt and storage through compounding and disposal. For non-hazardous sterile compounding, a horizontal laminar flow hood that meets USP <797> requirements is typically the appropriate choice. However, if your facility handles hazardous drugs as defined by USP <800>, you will need a containment primary engineering control such as a biological safety cabinet or a containment ventilated enclosure.

A horizontal laminar flow hood is the right choice when your compounding work involves non-hazardous sterile preparations that require product protection but do not pose an inhalation or exposure risk to the operator. Unlike a biosafety cabinet, which is designed to protect both the product and the user from hazardous materials, a horizontal laminar flow hood directs HEPA-filtered air toward the operator, making it unsuitable for any work involving hazardous drugs, cytotoxics, or biological agents. If your facility is compounding standard IV preparations, ophthalmic solutions, or other non-hazardous sterile compounds, a horizontal laminar flow hood offers a cost-effective, high-performance solution that meets USP <797> environmental requirements. Always verify the nature of the drugs being compounded before selecting your primary engineering control.