AE

2018

Choosing Engineering Controls Under USP 800

The risks to health care workers handling hazardous drugs (HDs) under non-USP compliant conditions are often underappreciated. The development of the USP 800 chapter provides a framework of 18 sections that guide HD compounding practices to ensure the safety not only of patients, but also of the health care workers who prepare and administer these […]

Choosing Engineering Controls Under USP 800 Read More »

The risks to health care workers handling hazardous drugs (HDs) under non-USP compliant conditions are often underappreciated. The development of the USP 800 chapter provides a framework of 18 sections that guide HD compounding practices to ensure the safety not only of patients, but also of the health care workers who prepare and administer these

StageThru 800

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. This equipment is designed to provide a protective barrier for the operator.  It is not iso-classified.  It

StageThru 800 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. This equipment is designed to provide a protective barrier for the operator.  It is not iso-classified.  It

Schedule Your On-site Facility Evaluation

Schedule Your On-site Facility Evaluation Last chance to set up an on-site meeting with our Pharmacy Projects Manager. Joe Skorcz will be on tour in the Minneapolis area performing visits for Aseptic Enclosures’ pharmacy design evaluations. If interested in scheduling a meeting and having our Engineer come and evaluate your facility’s day to day operations

Schedule Your On-site Facility Evaluation Read More »

Schedule Your On-site Facility Evaluation Last chance to set up an on-site meeting with our Pharmacy Projects Manager. Joe Skorcz will be on tour in the Minneapolis area performing visits for Aseptic Enclosures’ pharmacy design evaluations. If interested in scheduling a meeting and having our Engineer come and evaluate your facility’s day to day operations

XLTC800 for Tablet Pressing

  Here in Aseptic Enclosures we have encountered a project where we were called upon to come up with a solution that will provide ISO class 5 conditions for compounding tablets. The issues we had successfully overcome were: increasing safety of the pharmacist, assuring sterility of the product, limit particulate emissions and avoid risks for

XLTC800 for Tablet Pressing Read More »

  Here in Aseptic Enclosures we have encountered a project where we were called upon to come up with a solution that will provide ISO class 5 conditions for compounding tablets. The issues we had successfully overcome were: increasing safety of the pharmacist, assuring sterility of the product, limit particulate emissions and avoid risks for

Pharmacy Planning and Design Projects

  When it comes to clean room design, fabrication, installation, pricing, and customer service, we do clean rooms right. Whatever you’re looking for in a clean room, from economical soft wall installations to the top of the line hard wall construction for permanent use, our clean room value is second to none. We sell our

Pharmacy Planning and Design Projects Read More »

  When it comes to clean room design, fabrication, installation, pricing, and customer service, we do clean rooms right. Whatever you’re looking for in a clean room, from economical soft wall installations to the top of the line hard wall construction for permanent use, our clean room value is second to none. We sell our

Containing Bloodstream Infections

Pharmacy compounding is the process of combining drug ingredients to prepare medications that are not commercially available or to alter commercially available medications to meet specific patient needs such as dye-free or liquid formulations. Pharmacists traditionally have prepared medications to fulfill individual prescription requests or manipulated reasonable quantities of human drugs on receipt of a

Containing Bloodstream Infections Read More »

Pharmacy compounding is the process of combining drug ingredients to prepare medications that are not commercially available or to alter commercially available medications to meet specific patient needs such as dye-free or liquid formulations. Pharmacists traditionally have prepared medications to fulfill individual prescription requests or manipulated reasonable quantities of human drugs on receipt of a

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