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Aseptic Enclosures – Blog

Our XLTC 800 featured in the April Issue of PPP

  Our XLTC 800 isolator was featured in the latest issue of the PP&P Magazine who showcased our patent pending aseptic XLTC isolator that exceeds the minimum standards established by USP800.   A detailed overview of the XLTC800 and how it stands against the USP800 regulations is available on our site: https://asepticenclosures.com/usp800vxltc800/   Our company […]

Our XLTC 800 featured in the April Issue of PPP Read More »

  Our XLTC 800 isolator was featured in the latest issue of the PP&P Magazine who showcased our patent pending aseptic XLTC isolator that exceeds the minimum standards established by USP800.   A detailed overview of the XLTC800 and how it stands against the USP800 regulations is available on our site: https://asepticenclosures.com/usp800vxltc800/   Our company

Media Fill by Aseptic Enclosures

A media fill is the performance of an aseptic manufacturing procedure using a sterile microbiological growth medium, in place of the drug solution, to test whether the aseptic procedures are adequate to prevent contamination during actual drug production.   In aseptic processing, it is intended that a product and its containment system (separately sterilized) are brought together

Media Fill by Aseptic Enclosures Read More »

A media fill is the performance of an aseptic manufacturing procedure using a sterile microbiological growth medium, in place of the drug solution, to test whether the aseptic procedures are adequate to prevent contamination during actual drug production.   In aseptic processing, it is intended that a product and its containment system (separately sterilized) are brought together

Mobile Compounding Center Featured in PPP Magazine

  mobile compounding center featured in PPP Magazine in the latest issue of the PP&P Magazine who showcased our plug and play mobile cleanroom as this months’ new and noteworthy addition to the industry. Our mobile cleanroom modules are built to meet your specific ISO classification, pressure and venting requirements. They are delivered factory tested

Mobile Compounding Center Featured in PPP Magazine Read More »

  mobile compounding center featured in PPP Magazine in the latest issue of the PP&P Magazine who showcased our plug and play mobile cleanroom as this months’ new and noteworthy addition to the industry. Our mobile cleanroom modules are built to meet your specific ISO classification, pressure and venting requirements. They are delivered factory tested

Compounding Aseptic Containment Isolator from Aseptic Enclosures

We would like to start the New Year by introducing our Compounding Aseptic Containment Isolator. These close isolators provide a better physical barrier to protect the health of laboratory workers, maintain the sterility of experimental materials, and prevent the contamination of the environment. Closed containment cabinets are safer to use in research laboratories to provide a clean

Compounding Aseptic Containment Isolator from Aseptic Enclosures Read More »

We would like to start the New Year by introducing our Compounding Aseptic Containment Isolator. These close isolators provide a better physical barrier to protect the health of laboratory workers, maintain the sterility of experimental materials, and prevent the contamination of the environment. Closed containment cabinets are safer to use in research laboratories to provide a clean

Portable Compounding Cleanrooms

  Aseptic Enclosures, manufacturers of Portable Compounding Cleanrooms, in compliance with FDA, USP 797 & USP 800 standard. Many hospital pharmacies are undergoing major renovations to be in compliance with new standards. However, they must continue vital drug preparation without interruption. Aseptic Enclosures Mobile Cleanroom allows the hospital to maintain separate, on-site sterile drug compounding

Portable Compounding Cleanrooms Read More »

  Aseptic Enclosures, manufacturers of Portable Compounding Cleanrooms, in compliance with FDA, USP 797 & USP 800 standard. Many hospital pharmacies are undergoing major renovations to be in compliance with new standards. However, they must continue vital drug preparation without interruption. Aseptic Enclosures Mobile Cleanroom allows the hospital to maintain separate, on-site sterile drug compounding

Aseptic Enclosures in Attendance of Pack Expo Las Vegas 2017

  Aseptic Enclosures will be represented by Joe Skorcz, our new Project Engineer and Regional Manager.  Joe is directly responsible for Projects in our Northern Region, but will be available for requests concerning any region during the Pack Expo Las Vegas. At Aseptic Enclosures, we have a strong commitment to helping you improve your aseptic

Aseptic Enclosures in Attendance of Pack Expo Las Vegas 2017 Read More »

  Aseptic Enclosures will be represented by Joe Skorcz, our new Project Engineer and Regional Manager.  Joe is directly responsible for Projects in our Northern Region, but will be available for requests concerning any region during the Pack Expo Las Vegas. At Aseptic Enclosures, we have a strong commitment to helping you improve your aseptic

Cleaning Compounding Aseptic Isolators

  Using the right techniques and procedures can make cleaning sterile compounding areas a matter of routine. Since the June 1, 2008 revision of USP general chapter 797, pharmaceutical compounding personnel have been held responsible for the cleanliness of their sterile compounding areas, including biosafety cabinets (BSCs), compounding aseptic isolators (CAIs), compounding aseptic containment isolators

Cleaning Compounding Aseptic Isolators Read More »

  Using the right techniques and procedures can make cleaning sterile compounding areas a matter of routine. Since the June 1, 2008 revision of USP general chapter 797, pharmaceutical compounding personnel have been held responsible for the cleanliness of their sterile compounding areas, including biosafety cabinets (BSCs), compounding aseptic isolators (CAIs), compounding aseptic containment isolators

Why Sterile Alcohol?

  FDA reminder of safe non sterile alcohol prep pad use The FDA is reminding healthcare professionals about the safe use of non-sterile alcohol prep pads to clean and disinfect the surface of the skin. This reminder comes in light of the recent recall of Triad Group alcohol prep pads and swabs due to concerns

Why Sterile Alcohol? Read More »

  FDA reminder of safe non sterile alcohol prep pad use The FDA is reminding healthcare professionals about the safe use of non-sterile alcohol prep pads to clean and disinfect the surface of the skin. This reminder comes in light of the recent recall of Triad Group alcohol prep pads and swabs due to concerns

Case Study: Hospital Upgrades Cleanroom

Here’s a case study about a customer that saved a lot of time and money by implementing Aseptic Enclosures’ HEPACirc™ for their facility. Aseptic Enclosures’ HEPACirc™ is a general-purpose, “Plug-and-Play” Clean Room Grade, air purification upgrade system ideally suited to many types of clean mechanical or processing work. It is designed to provide an ISO

Case Study: Hospital Upgrades Cleanroom Read More »

Here’s a case study about a customer that saved a lot of time and money by implementing Aseptic Enclosures’ HEPACirc™ for their facility. Aseptic Enclosures’ HEPACirc™ is a general-purpose, “Plug-and-Play” Clean Room Grade, air purification upgrade system ideally suited to many types of clean mechanical or processing work. It is designed to provide an ISO

Clean Room Experts

The basic function of a clean room is to protect the manufactured product from contamination. In  pharmaceutical production, the survival of a drug manufacturer is heavily invested the safety of the finished product. So, it is necessary to identify any potential source of contamination, which includes the working environment itself. Requirements of the quality of

Clean Room Experts Read More »

The basic function of a clean room is to protect the manufactured product from contamination. In  pharmaceutical production, the survival of a drug manufacturer is heavily invested the safety of the finished product. So, it is necessary to identify any potential source of contamination, which includes the working environment itself. Requirements of the quality of