AE

Compounding

Aseptic Enclosures – Compounding

TPN compounding

Making TPN Compounding Safe

In the last couple of years, in an effort of Making TPN compounding safe, we have recorded a serious upswing and increase in the 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 […]

Making TPN Compounding Safe Read More »

In the last couple of years, in an effort of Making TPN compounding safe, we have recorded a serious upswing and increase in the 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

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

TPN compounding

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.

Aseptic Compounding

Excluding Contamination in Aseptic Compounding

Steroids for epidural delivery were found to be contaminated with fungal spores leading to over 700 reported cases of meningitis and 64 deaths.

Excluding Contamination in Aseptic Compounding Read More »

Steroids for epidural delivery were found to be contaminated with fungal spores leading to over 700 reported cases of meningitis and 64 deaths.

ON-SITE EVALUATION OF FACILITY

  When it comes to cleanroom design, fabrication, installation, pricing, and customer service, we do clean rooms right. 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

ON-SITE EVALUATION OF FACILITY Read More »

  When it comes to cleanroom design, fabrication, installation, pricing, and customer service, we do clean rooms right. 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

Preventing Contamination In Compounding Facilities

Compounding pharmacies come in many different shapes and sizes. They can consist of a pharmacist creating a drug under a doctor’s prescription or they can be pharmacy-type facilities that compound drugs and sell them like a manufacturer. Sporadic and serious infection outbreaks have been linked to compounding pharmacies outside of the hospital setting.1 These problems date

Preventing Contamination In Compounding Facilities Read More »

Compounding pharmacies come in many different shapes and sizes. They can consist of a pharmacist creating a drug under a doctor’s prescription or they can be pharmacy-type facilities that compound drugs and sell them like a manufacturer. Sporadic and serious infection outbreaks have been linked to compounding pharmacies outside of the hospital setting.1 These problems date

Updated Guidance for Compounding Facilities 503B

The Food and Drug Administration (FDA or the Agency) is announcing the availability of a revised draft guidance entitled “Current Good Manufacturing Practice—Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act.” This revised draft guidance describes FDA’s policies regarding compounders registered under section 503B of the Federal Food, Drug, and

Updated Guidance for Compounding Facilities 503B Read More »

The Food and Drug Administration (FDA or the Agency) is announcing the availability of a revised draft guidance entitled “Current Good Manufacturing Practice—Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act.” This revised draft guidance describes FDA’s policies regarding compounders registered under section 503B of the Federal Food, Drug, and