AE

Compounding Solutions

Aseptic Enclosures – Compounding Solutions

In case you missed the presentation we did a few days ago on "How to get a clean-room designed, built, and certified in less than 5 months

How to get a clean-room designed, built and certified in less than 5 months

In case you missed the presentation we did a few days ago on “How to get a clean-room designed, built, and certified in less than 5 months which will have a ‘Plug and Play’ feature for permanent or temporary installations “, we now have the recordings available for on-demand review. In this presentation, we review the […]

How to get a clean-room designed, built and certified in less than 5 months Read More »

In case you missed the presentation we did a few days ago on “How to get a clean-room designed, built, and certified in less than 5 months which will have a ‘Plug and Play’ feature for permanent or temporary installations “, we now have the recordings available for on-demand review. In this presentation, we review the

Compounding Capabilities during Cleanroom Renovations

Compounding Capabilities during Cleanroom Renovations

When renovating a cleanroom, or creating one from non-cleanroom space, understanding the details — of the site, building, planned research, and equipment — is essential. Cleanrooms are like race cars. When properly designed and built, they are highly efficient performance machines. When poorly designed and built, they operate poorly and are unreliable. The cost of cleanroom varies

Compounding Capabilities during Cleanroom Renovations Read More »

When renovating a cleanroom, or creating one from non-cleanroom space, understanding the details — of the site, building, planned research, and equipment — is essential. Cleanrooms are like race cars. When properly designed and built, they are highly efficient performance machines. When poorly designed and built, they operate poorly and are unreliable. The cost of cleanroom varies

pass through chamber

WHAT IS A PASS THROUGH CHAMBER?

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.

WHAT IS A PASS THROUGH CHAMBER? 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.

Compounding Capabilities during Cleanroom Renovations

How should we Keep Cleanrooms Clean?

Controlling microbial ingress into the cleanroom is a critical concern for the entire cleaning and disinfection process. Components, personnel, carts, tanks, tools, cleaning supplies, and instruments that are transferred into the clean area should be clean and free of contamination. Cross contamination is easier to prevent than to correct.

How should we Keep Cleanrooms Clean? Read More »

Controlling microbial ingress into the cleanroom is a critical concern for the entire cleaning and disinfection process. Components, personnel, carts, tanks, tools, cleaning supplies, and instruments that are transferred into the clean area should be clean and free of contamination. Cross contamination is easier to prevent than to correct.

Can an Isolator still be used without a Cleanroom?

Can an Isolator still be used without a Cleanroom?

Can an Isolator still be used without a Cleanroom? The answer is complicated. Under the current USP 797 guidelines, a compounding aseptic isolator may be used as a substitute for a cleanroom if it is certified to meet ISO 5 under dynamic conditions. Usually, the certifier will conduct particle tests and airflow studies while a

Can an Isolator still be used without a Cleanroom? Read More »

Can an Isolator still be used without a Cleanroom? The answer is complicated. Under the current USP 797 guidelines, a compounding aseptic isolator may be used as a substitute for a cleanroom if it is certified to meet ISO 5 under dynamic conditions. Usually, the certifier will conduct particle tests and airflow studies while a

Compounding Capabilities during Cleanroom Renovations

The Risks of Automated Compounding of IV Products

The last couple of years we have recorded a serious upswing and increase of use of automated IV preparation systems. Their popularity is directly linked to their ease of use since they combine barcode scanning and Digital image capture to ensure safer and more efficient compounding processes. With the increase of use of such technology

The Risks of Automated Compounding of IV Products Read More »

The last couple of years we have recorded a serious upswing and increase of use of automated IV preparation systems. Their popularity is directly linked to their ease of use since they combine barcode scanning and Digital image capture to ensure safer and more efficient compounding processes. With the increase of use of such technology