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...
View ArticleHow 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...
View ArticleCleanroom 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 —...
View ArticleCleanroom 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,...
View ArticleEntering a Cleanroom: Preparation and Procedure – The Garments Employees Must...
This guide provides a framework for employees entering a cleanroom.
View ArticleCleanroom Classification Comparison Specifications Defined
A comparison of cleanroom classifications and specifications.
View ArticleCleanroom 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,...
View ArticleSoftwall Cleanroom Enclosure
This customer needed to enclose a piece of machinery, and CleanPro® was able to provide a solution.
View ArticleCleanPro® Stand Alone Hardwall Cleanroom
CleanPro’s modular hardwall cleanroom solutions adapt alongside changing floor and production layouts.
View ArticleClass 10,000 Cleanroom & Gowning Area
This cleanroom and adjacent gowning area helped this customer prevent outer contamination from entering classified spaces.
View ArticleChemotherapy 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...
View ArticleClean-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...
View ArticleSoftwall 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...
View ArticleTurnkey 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,...
View ArticleFingerprints 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...
View ArticleCannabis 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...
View ArticleCleanroom 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...
View ArticleCleanroom and Sterile Compounding Glossary and Definitions
The definitive cleanroom and sterile compounding glossary. Learn terminology and definitions for USP 797 and USP 800 compounding.
View ArticleHow 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...
View ArticleUpgrading 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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