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Every transitional stage requires changes to the processing equipment and cleaning techniques. Discover the importance of proper cleaning to prevent contamination with various methods for cleaning pharmaceutical manufacturing equipment including manual, spray, and immersion Clean-in-Place (CIP) systems.
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A cleaning validation study involves testing manufacturing surfaces to ensure that they are being cleaned to an acceptable level of residue, documenting that testing data, and establishing procedures to maintain that level of cleanliness. Explore the steps involved in cleaning validation and what it provides for manufacturers.
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Selecting an aqueous cleaning system that includes a cleaning method, rinse method, and drying method is crucial. Delve into this chapter of The Aqueous Cleaning Handbook and walk through a seven-step process to help you optimize your cleaning process.
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Process optimization is key to achieving effective pharmaceutical and cosmetic critical cleaning. By using the right cleaning agents, optimizing cleaning parameters, and implementing thorough validation procedures, manufacturers can improve cleaning efficiency and ensure safety.
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Surface cleaning or degreasing can be defined as the removal of residues. Explore this chapter of The Aqueous Cleaning Handbook as it explains what an aqueous cleaner is, what it contains, and how it can improve your cleaning process. Additionally, discover the various types of cleaning agents and take a look at the history of each.
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Critical cleaning is the removal of unintended residue. Review a guide that is intended to assist laboratory, manufacturing plant scientists, and engineers in accurately selecting and maximizing the performance of aqueous cleaners and systems. You will find handy, easy-to-read summaries of what aqueous cleaning is and how it works.
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It is important to have clean laboratory equipment, as any “leftover” proteins, RNA, or DNA could potentially contaminate your next experiment. Learn about three of the best methods for cleaning proteins, RNA, and DNA from lab equipment.
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FDA-Registered Detergents
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All Alconox Inc. detergents are Class I Medical Devices and listed as FDA-registered detergents. The full list of detergents can be found on the FDA website with FDA Registration number 2410887. Alconox Inc. is also proud to be ISO9001:2015 and ISO13485:2016 Certified.
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• Request Information
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Proper cleaning chemistry is critical for preventing contamination, ensuring product quality, and meeting regulatory standards. Join us March 25th as we explore how selecting the appropriate cleaning agents, optimizing parameters such as temperature, time, and concentration, and implementing thorough validation procedures, manufacturers can enhance cleaning efficiency and ensure product safety.
Click here to register.
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