ABOUT CONTEC
Mission-Critical Cleaning for Contamination Control
Contec is the leading manufacturer of contamination control products for critical cleaning and manufacturing environments worldwide. Our innovative wipes, mops, and solutions are used in various industries across the globe.
VIDEOS
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Effective cleanroom management requires moving beyond checkbox compliance. Learn how to empower your workforce by connecting individual roles to broader contamination control goals and behaviors.
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Achieving sterile excellence requires more than just rigid protocols. Learn how to foster a proactive mindset across your entire organization to ensure long-term facility integrity.
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Ensure cleanroom compliance by aligning disinfectant validation with real-world application methods. Learn to justify your protocols and adapt to facility changes through expert technical insights.
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Discover the proper mopping techniques when using a 3-bucket system through an in-depth demonstration and detailed instructions.
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Improper wiping techniques do not remove contaminants reliably or effectively. From a detailed demonstration, learn the proper wiping technique for critical environments.
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Learn the proper mopping techniques when using a 2-bucket system through a detailed demonstration and step-by-step instructions.
CONTACT INFORMATION
Contec, Inc.
P.O. Box 530
Spartanburg, SC 29304
UNITED STATES
FEATURED ARTICLES
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Move beyond raw data by using heat maps and site-specific limits to identify contamination hotspots. Transform your environmental monitoring into a proactive strategy for operational excellence.
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Keeping your cleanroom spotless is vital for product quality and patient safety. Consider these important factors for how to build a culture of clean and how your cleanroom will benefit.
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Environmental monitoring (EM) is essential, but it’s only part of the picture. Discover why a proactive contamination control strategy is key to keeping your cleanroom truly audit-ready.
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Gene therapy manufacturing demands a careful balance between contamination control and efficiency. A strategic approach to “critical aseptic” designation is essential to meet evolving regulatory challenges.
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Minimizing endotoxin contamination is vital in pharmaceutical manufacturing to protect patients from harmful reactions. Learn more about rigorously tested, low-endotoxin products designed for critical cleanroom and sterile applications.
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Effective isolator cleaning is crucial for vapor phase hydrogen peroxide (VPHP) decontamination. Proper tools, techniques, and training ensure sterility, and regulatory compliance.
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Explore Annex 1 updates on contamination control in pharmaceutical cleanrooms, emphasizing cleaning consistency, training, advanced tools, and technologies to achieve regulatory compliance.
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Explore effective strategies and cleaning supplies to ensure irregular cleanroom surfaces, such as light switches, door handles, valves, and piping, maintain the same standards as more accessible areas.
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Considering ergonomics is crucial for optimizing cleaning efficiency and minimizing contamination risks. Explore key ergonomic considerations in cleanroom cleaning, best practices, and more.
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Learn why proper training is vital in cleanroom cleaning and disinfection and how to develop and maintain a successful training initiative.
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Explore the challenges presented by the residues left behind by disinfectant solutions in cleanrooms as well as effective strategies for their management.
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Learn about the significance of residue removal, how it is effectively performed in cleanrooms to ensure the compliance of biosafety cabinets, and the impact of proper residue removal.
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Learn about the problems caused by residues left behind by disinfectant solutions, challenges to residue removal in cleanrooms, and effective removal techniques for ongoing residue management.
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Learn about the three cleaning best practices that will make a difference in your cleanroom, the importance of each step, and how to implement these strategies.
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Explore the most recent rewrite of the EU Annex 1 document as well as the contamination control strategy outlined within.
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The new GMP regulations coming out of the European Union will have a big impact on pharmaceutical manufacturers. Learn about executing a CSS, cleaning, disinfection, and much more.
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A systematic approach determines the best disinfectant solution for a facility. Learn about the variables that impact disinfection of surfaces, including tool selection and the application of disinfectant solutions.
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A clear understanding of mopping best practices is needed to make informed decisions that improve cleanroom maintenance while controlling costs. Learn about mopping coverage, systems, and validation.
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The reuse of mops should be carefully considered. Explore microfiber, the difference between relaundered microfiber mops and single-use disposable microfiber products, and more.
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Learn why it is not possible to definitively categorize or certify wipes for a specific class of cleanroom environment.