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Channel: Definitive Clean Room Guide - Cleanroom Standards, Classifcation, and Protocol
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Cleanroom Cleaning, Gowning, and Maintenance — Procedure, Contamination...

Proper cleanroom cleaning procedure and maintenance protocol is an immediate, low-cost measure to enhance overall cleanliness, consistency, and contamination control within manufacturing and aseptic...

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How to Choose the Right Cleanroom Particle Counter

Cleanroom particle counters differ widely based upon particle threshold, cost, and features. How to do you determine if you need a particle counter or what model of particle counter to purchase? In...

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Cleanroom Components — Air Filtration, Design, and Other Variables

What are the key determinants of cleanroom components? Learn about different types of cleanroom filtration, wall construction, lights, temperature, humidity and more. The post Cleanroom Components —...

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Cleanroom Installation Examples by CleanPro®

Here are some best-in-class cleanroom projects, in which the PAC cleanroom division, CleanPro, provided expertise and turnkey execution for design and installation of cleanroom enclosures, furniture,...

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Entering a Cleanroom: Preparation and Procedure – The Garments Employees Must...

This guide provides a framework for employees entering a cleanroom.

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Cleanroom Classification Comparison Specifications Defined

A comparison of cleanroom classifications and specifications.

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Cleanroom HEPA Vacuum Use and Applications 

Cleanroom HEPA Vacuum Components and Applications Simply put, every square inch of a cleanroom should be absolutely pristine. Ceiling panels, lighting units, HEPA filtration units, sprinkler heads,...

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Softwall Cleanroom Enclosure

This customer needed to enclose a piece of machinery, and CleanPro® was able to provide a solution.

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CleanPro® Stand Alone Hardwall Cleanroom

CleanPro’s modular hardwall cleanroom solutions adapt alongside changing floor and production layouts.

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Class 10,000 Cleanroom & Gowning Area

This cleanroom and adjacent gowning area helped this customer prevent outer contamination from entering classified spaces.

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Chemotherapy and CSP Cleanroom Installation

This modular, sterile compounding cleanroom is designed for ISO 797 and ISO 800 compliance, particularly for compounding chemotherapy drugs. Safe handling of sterile compounds requires special...

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Clean-Forward Lab Furniture Project

Industrial workbenches and workstations provide integrated design features such as power bars, application specific surface materials, and custom drawer and cabinet configurations for safe, organized...

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Softwall Cleanroom Curtains Project

Softwall cleanroom curtains, sometimes referred simply as “plastic strips” yield ISO Class 10,000 level particle control with minimal construction. This customer required a custom softwall installation...

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Turnkey Cleanroom Install

CleanPro’s turn-key cleanroom solution provided a one-stop, one-contact result for the initial delivery and on-site installation of walls, ceiling grids, electrical systems, flooring, filters, HVAC,...

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Fingerprints of a Killer: Why Medicinal Cannabis Needs a Cleanroom Engineered...

The benefit of modular cannabis cleanrooms over traditional fixed wall grow rooms is that the configurable partitions of modular cleanroom designs lower the cost of installation or re-configuration for...

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Cannabis Cleanroom Design and Construction Components

This post regards the specific construction components of building a cleanroom for medical cannabis cultivation. Previously, we’ve written about the dangers of contaminated cannabis, and how it affects...

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Cleanroom Construction FAQ

Definitive Cleanroom Construction FAQ: How much does a cleanroom cost? How does the level of ISO classification impact build and operating costs? How much supporting space will I need for a cleanroom...

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Cleanroom and Sterile Compounding Glossary and Definitions

The definitive cleanroom and sterile compounding glossary. Learn terminology and definitions for USP 797 and USP 800 compounding.

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How Does USP 800 Change Storage and Unpacking of Hazardous Drugs?

Facilities unpacking hazardous drugs within a negative pressure room do not require procedural changes to meet USP unpacking area requirements. Facilities unpacking HDs within positive pressure ante...

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Upgrading a USP 797 Cleanroom to USP 800?

New USP guidelines may present challenges for compounding facilities. Some facilities need infrastructural and mechanical modifications for compliance. System evaluation includes duct systems, HEPA fan...

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