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Why Sterile Alcohol?

Leave a Comment / Blog, Company News, Compounding News, FDA News, Hospital Industry News, Pharmaceutical Industry News, Research News, Store /

Monday April 10, 2017

  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

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Monday January 16, 2017

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

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Wednesday December 21, 2016

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

Sterile Compounding: A Guide for Community Pharmacists

5 Comments / Blog, Compounding News, Literature, Pharmaceutical Industry News /

Friday December 9, 2016

After reading this article you will: understand the principles of sterile compounding understand the requirements for sterile compounding understand the principles of operation of a laminar airflow hood Introduction Health care is increasingly moving into the home setting, creating new challenges for pharmacists. Pharmacists may be asked to fill prescriptions for intravenous solutions, and prepare

Sterile Compounding: A Guide for Community Pharmacists Read More »

After reading this article you will: understand the principles of sterile compounding understand the requirements for sterile compounding understand the principles of operation of a laminar airflow hood Introduction Health care is increasingly moving into the home setting, creating new challenges for pharmacists. Pharmacists may be asked to fill prescriptions for intravenous solutions, and prepare

We help you Create Aseptic and Safest Environment!

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Tuesday November 29, 2016

Is your hospital affiliated with Premier, Inc?  Aseptic Enclosures is a contracted supplier through Premier Inc.  Our two agreements with Premier; Pharmacy Planning and Conceptual Design and Primary Engineering Control Devices, allow us to help you achieve USP 800 and USP 797 compliance with the savings of Premier membership.  With all the ever-changing rules compliance

We help you Create Aseptic and Safest Environment! Read More »

Is your hospital affiliated with Premier, Inc?  Aseptic Enclosures is a contracted supplier through Premier Inc.  Our two agreements with Premier; Pharmacy Planning and Conceptual Design and Primary Engineering Control Devices, allow us to help you achieve USP 800 and USP 797 compliance with the savings of Premier membership.  With all the ever-changing rules compliance

Environmental Sampling Test Supplies

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Thursday October 20, 2016

USP <797> outlines three risk levels for compounding sterile preparations: low, medium, and high. The risk level is determined based on the likelihood of contamination, the number of manipulations involved in compounding, and the environment in which compounding occurs. For low-risk compounding, which involves aseptic manipulations using only sterile components and equipment, the minimum requirement

Environmental Sampling Test Supplies Read More »

USP <797> outlines three risk levels for compounding sterile preparations: low, medium, and high. The risk level is determined based on the likelihood of contamination, the number of manipulations involved in compounding, and the environment in which compounding occurs. For low-risk compounding, which involves aseptic manipulations using only sterile components and equipment, the minimum requirement

Aseptic Enclosures Lunch and Learn Meetings For Your State BOP

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Thursday October 13, 2016

Aseptic Enclosures has been traveling across the United States to bring State Boards of Pharmacy the latest updates and innovations for USP 797 and USP 800 compliance while providing lunch for the day! Call us or Live chat us today to schedule your State Board of Pharmacy Lunch and Learn!  Aseptic Enclosures has decades of

Aseptic Enclosures Lunch and Learn Meetings For Your State BOP Read More »

Aseptic Enclosures has been traveling across the United States to bring State Boards of Pharmacy the latest updates and innovations for USP 797 and USP 800 compliance while providing lunch for the day! Call us or Live chat us today to schedule your State Board of Pharmacy Lunch and Learn!  Aseptic Enclosures has decades of

First Air principle

The importance of first air principle in aseptic processing and sterile compounding

3 Comments / Blog, Compounding News, Featured, Pharmaceutical Industry News /

Monday April 11, 2016

“First air principle is the last defense against contamination, that’s why The importance of first air principle in aseptic processing and sterile compounding is very high” It can help guard against bad technique being utilized in upstream processes. The USP goes to great lengths to describe first air and unidirectional airflow. Significant testing and airflow

The importance of first air principle in aseptic processing and sterile compounding Read More »

“First air principle is the last defense against contamination, that’s why The importance of first air principle in aseptic processing and sterile compounding is very high” It can help guard against bad technique being utilized in upstream processes. The USP goes to great lengths to describe first air and unidirectional airflow. Significant testing and airflow

USP 800 policy Usp 800 Report

USP 800 Policy

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Thursday February 4, 2016

USP Publishes Standard on Handling Hazardous Drugs in Healthcare Settings Rockville, Md., February 1, 2016—The United States Pharmacopeial Convention (USP) published today an important new standard as part of a suite of healthcare quality standards included in the United States Pharmacopeia-National Formulary (USP-NF). USP 800 policy of Hazardous Drugs Management: The new general chapter,  USP

USP 800 Policy Read More »

USP Publishes Standard on Handling Hazardous Drugs in Healthcare Settings Rockville, Md., February 1, 2016—The United States Pharmacopeial Convention (USP) published today an important new standard as part of a suite of healthcare quality standards included in the United States Pharmacopeia-National Formulary (USP-NF). USP 800 policy of Hazardous Drugs Management: The new general chapter,  USP

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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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