In the world of biodecontamination, one of the most persistent and misleading myths is that higher hydrogen peroxide (H2O2) concentrations automatically mean better performance. This misconception continues to be fueled by legacy biodecontamination...
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In the pharmaceutical industry, protecting SISPQ—Safety, Identity, Strength, Purity, and Quality—is the cornerstone of compliance. “Throughout the development and release of a commercial product, a critical part of Chemistry, Manu...
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Aseptic environments prevent microbial contamination in pharmaceutical, healthcare, and laboratory settings. These controlled spaces ensure that even the smallest compromise in sterility does not jeopardize patient safety, product efficacy, or rese...
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June is Safety Month, and here at CURIS, we thought it would be the perfect time to highlight how Smart Disinfection can significantly boost laboratory safety. But what exactly is Smart Disinfection? Smart Disinfection refers to the integration ...
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Sterility testing is a critical process across pharmaceutical, research, and clinical laboratories. It ensures that products, environments, and tools meet the strict requirements for sterility to prevent contamination risks and protect public healt...
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A laboratory’s reliability hinges on its cleanliness, including contamination control. Whether in a research or medical setting, sterility serves as the backbone of effective work and accurate results. Beyond just appearances, a thoroughly di...
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Laboratory facilities are built on the foundation of product safety and contamination control. Whether it’s a research lab, clean room, or public health laboratory, ensuring sterility in such environments isn't just important—it's criti...
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In the complex world of life sciences and pharmaceutical manufacturing, choosing the right bio-decontamination system for transfer environments can significantly impact a facility's efficiency, compliance, and bottom line. As technology advances an...
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The integrity of scientific research, public health testing and surveillance, and pharmaceutical product development hinges on one fundamental principle: ensuring the highest levels of sterility. Effective disinfection and sterilization are vital t...
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A recent article in Bioprocess Online comparing vaporized and aerosolized hydrogen peroxide bio-decontamination methods has sparked important discussions in the bio-decontamination technology space. The article raises valid points about the limitat...
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Misconception #1: "Mold Spores Are the Standard for Sterilization" There's a misconception floating around that mold spores (fungal spores) are the gold standard for validating sterilization processes. Let's set the record straight: bacteria...
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The cleanroom stands as a bastion against contamination in the world of laboratories and medical facilities, ensuring that you and your team always conduct research and healthcare activities in the most sterile environment possible. Yet, maintainin...
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In the high-stakes world of cleanrooms, laboratories, and GMP facilities, two microscopic challengers reign supreme: bacterial spores and fungal spores. While both can strike fear into the hearts of facility managers, understanding their difference...
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Hydrogen peroxide has emerged as the premier choice for biodecontamination, prompting facilities to explore low-concentration systems that avoid the safety and material compatibility issues inherent in higher-percentage solutions. While these gentl...
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In the world of pharmaceutical manufacturing, maintaining GMP/cGMP standards is essential. Facility managers, operations directors, and quality engineers continually face the challenge of optimizing production while ensuring the highest levels of saf...
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Ethylene Oxide, more commonly known as ETO, is a high-level disinfectant used for many years for sterilization of medical devices due to its ability to effectively eliminate many pathogens. However, recent investigations by the U.S. Environmental P...
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What is Avian Influenza (H5N1)? Avian influenza, commonly known as bird flu (H5N1), is a highly pathogenic virus that causes influenza in birds and other animals and leads to high mortality rates. First discovered in Italy in 1878 when reports of ...
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How CURIS System Avoids Corrosion and Rust While Ensuring Effective Decontamination When it comes to laboratory bio-decontamination, material compatibility and surface safety are critical factors that can significantly impact your facil...
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A materials transfer protocol is an essential process of a containment laboratory and or cleanroom environment where the required movement of materials from one classified space to another is performed safely* and efficiently without contaminati...
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The role of disinfectants is pivotal in maintaining contamination control and germ-free facilities. With increasing awareness and demand for effective disinfection methods, particularly due to recent global health concerns, understanding the nuances ...
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Introduction A recent discovery at a South Carolina beef processing plant raised new questions about a poorly understood pathogenic agent known for causing swift onset dementia and the buildup of amyloid fibers in the brain that cause Swiss cheese-l...
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Are BIs the Validation Tool for You? Biological indicators (BIs) containing Geobacillus stearothermophilus have become a standard and reliable source in the world of high-level disinfection and sterilization. These tools provide valuable information...
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The Changing Landscape, Same Fundamental Needs It’s been a rollercoaster ride since the COVID-19 pandemic first reared its head, but some things remain unchanged. The need for fast, easy, and effective disinfection methods with a reliable supp...
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A Look at Regulatory Compliance for Sporicides There are multiple guidelines in the updated Annex I specifying the use of a sporicidal agent for sterile manufacturing procedures in cleanrooms, isolators, and RABs, but what delineates a sporicidal ag...
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Environmental monitoring is a universal process and has been implemented in many industries, including laboratories, cleanroom pharmaceutical manufacturing facilities, the medical device industry, and even hospitals. The samples collected during this...
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