Pharmaceutical Industry News Archives | Page 6 Of 7

Aseptic Enclosures in Attendance of Pack Expo Las Vegas 2017

Friday August 25, 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 […]

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Cleaning Compounding Aseptic Isolators

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Wednesday April 19, 2017

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

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Why Sterile Alcohol?

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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

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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

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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

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Sterile Compounding: A Guide for Community Pharmacists

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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

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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

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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

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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

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Hospital Upgrades Cleanroom

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Saturday June 18, 2016

The Situation: A Hospital Upgrades Cleanroom that was not meeting the USP<797> requirements(1) for an ISO class 7 (2) grade cleanroom. The existing cleanroom was deficient in both Air Changes Per Hour (ACPH) and lacked low wall returns. The Challenge: After multiple meetings with pharmacy staff, facilities, maintenance, engineering and architectural, it was determined that

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