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Latest from Cleanroom News

Ensuring Cleanroom Compliance: The Pillar of Safe and High-Performing Manufacturing

In the world of pharmaceutical manufacturing, biotechnology, and advanced material production, cleanrooms serve as the backbone of contamination control. However, designing and maintaining a compliant cleanroom is not just about meeting regulatory expectations—it is about ensuring safe, consistent, and high-quality manufacturing processes.

Nelson Labs Launches Innovative Rapid Sterility Testing in Laboratories in the U.S.A and Europe

Nelson Labs, a global leader in microbiological and analytical chemistry testing, has unveiled its cutting-edge Rapid Sterility Testing service, an innovation poised to significantly expedite product release timelines for pharmaceutical and medical device manufacturers.

Clarios Announces $6 Billion Investment in Energy Manufacturing Strategy

Clarios, the Wisconsin-based global leader in low-voltage energy storage, announced a $6 billion plan expected to expand U.S. manufacturing and accelerate American innovation. The plan aims to advance American energy and critical mineral independence by strengthening the nation’s critical supply of batteries essential to start every vehicle in the U.S. The plan would expand existing operations, build new facilities, unlock innovation and create American jobs enabled by recent executive orders and using federal advanced manufacturing tax credits.

Eli Lilly U.S. Manufacturing Investment to Exceed $50 Billion

Eli Lilly and Company announced plans to bolster its domestic medicine production across therapeutic areas by building four new pharmaceutical manufacturing sites in the United States.

Thermo Fisher Scientific to Acquire Solventum’s Purification and Filtration Business

Thermo Fisher Scientific Expands Bioprocessing Capabilities with $4.1 Billion Acquisition of Solventum’s Purification & Filtration Business Thermo Fisher Scientific Inc. (NYSE: TMO), a global leader in serving science, has announced a definitive agreement to...
USP 797 Cleanroom Performance

USP 797 Cleanroom Performance

USP General Chapter <797> provides standards for compounding sterile preparations to promote patient safety and prevent harm. These standards help ensure patients receive quality preparations that are free from contaminants and are consistent in intended identity, strength and potency.

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Global Cleanroom Technology Market

Global Cleanroom Technology Market: Increasing Demand from Pharmaceutical and Medical Devices Industries to Push Market Growth at 5.2% CAGR The global cleanroom technology market was estimated to be USD 3,156.0 million in 2014. It is likely to grow at a CAGR of 5.2%...

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Global Clean Room Technology Market

Global Clean Room Technology Market

The global clean room technology market was estimated to be USD 3,156.0 million in 2014. It is likely to grow at a CAGR of 5.2% from 2014 to 2020, and reach a value of over USD 4,290 million by 2020.

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Clean Room Sticky Mats

Clean Room Sticky Mats

What type of sticky mat is right for my cleanroom? Clean Room Sticky Mats that are machine washable as well as peel up sticky mats come in a variety of types, sizes and prices. Selecting the appropriate type of mat for your modular cleanroom environment will depend on...

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Washable Sticky Mats vs. Disposable Sticky Mats

What type of sticky mat is right for my cleanroom? Sticky mats that are machine washable as well as peel up sticky mats come in a variety of types, sizes and prices. Selecting the appropriate type of mat for your modular cleanroom environment will depend on the type...

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What are cleanroom classifications?

Cleanrooms are classified by how clean the air is. In Federal Standard 209 (A to D) of the USA, the number of particles equal to and greater than 0.5mm is measured in one cubic foot of air, and this count is used to classify the cleanroom. This metric nomenclature is...

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