Aseptic Enclosures – Compounding News
Pharmaceutical compounding involves the preparation of medications tailored to the specific needs of individual patients. However, the process of pharmaceutical compounding is complex, and the products must be sterile and meet strict quality standards. The USP <797> guidelines set out the requirements for sterile compounding, and a designated person is responsible for ensuring compliance with …
1) Temporary and Rental options: Primary Engineering controls: We have a range of Solutions for Pharmacy Cleanroom Renovations. CAI and CACI’s are available for rent (or purchase). These isolator units can be installed outside of a cleanroom while remaining compliant to current USP 797 guidelines without a reduction of the products beyond use …
Three Simple Solutions for Pharmacy Cleanroom Renovations: Read More »
Under the USP 800, an anteroom is defined as “An ISO Class 7 or cleaner room” where personnel hand hygiene, garbing procedures, and other activities that generate high particulate levels are performed. The ante-room is the transition room between the unclassified area of the facility and the buffer room. USP 800 requires ante-rooms to produce …
The consequences might be fatal for the personnel that handles HDs on daily basis in the R&D laboratories. Safer Compounding Solutions provides complete protection because It has built with a strong engineering control. Isolators: Our XLTC isolator isolates the personnel from the HD exposure that might happen in the process of compounding pharmaceuticals for …
The importance of understanding your current situation is always a great starting point for any type of project. So our pharmacy project engineers are now conducting on-site visits for inspection and evaluation of your cleanroom areas in your facility.
Developing an effective compounding strategy is critical to ensuring patients have access to properly compounded medications, but because each organization’s needs differ, a one-size-fits-all solution cannot be applied to every hospital. A careful evaluation of the institution’s requirements, the available infrastructure for compounding medications in-house, and any registered 503B compounding facilities in the vicinity with …
Although most pharmacy personnel will say that the highest risk of exposure to hazardous drugs is during the compounding process, we feel that there is an even greater risk of exposure to hazardous materials during shipping and receiving. Under the current regulations as well as the upcoming USP <800> the hazardous materials are usually ordered …
Introduction: The use of chemotherapy drugs in cancer treatment has increased significantly in recent years. However, concerns have been raised regarding the potential risks to employees who work in chemo clinics and their fertility and pregnancy. In this article, we will examine the impact of chemotherapy on fertility and pregnancy and how to ensure a …
Whether isolator or cleanroom-based working areas, if we’re talking about both sterile and hazardous sterile preparations we recognize the first source of Exposure To Hazardous Materials . The first known is actually outside of the cleanroom and is the pre-cleaning station. In the hazardous drug area, we like to see packages from shipping and receiving brought …
Exposure to Hazardous Materials during Shipping and Receiving Read More »
The StageThru800 is a negative pressure, isolated, Pass-through, CVE (Containment Ventilated Enclosure) device that is intended to provide a significantly safer way for incoming shipments to be staged and prepped for entry into the hazardous drug compounding area.
Aseptic Enclosures located in St Louis, Missouri manufactures a wide range of Air Filtration equipment for Aseptic processing and Containment applications.
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Central Time, Monday-Friday
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