Abstract
Sterilization is a critical aspect of the medical device industry, as the use of improperly sterilized devices can have serious consequences for patients. This article provides an overview of the risks of inadequate sterilization, the methods of sterilization commonly used in the industry, and best practices for ensuring safe and effective sterilization. The article also explores emerging sterilization technologies and their potential impact on the industry. The importance of quality assurance and control procedures, validation, and testing in the sterilization process is emphasized. By following best practices and staying up-to-date with technological advancements, the medical device industry can continue to ensure that sterilization is performed safely and effectively to protect patients and maintain industry standards.
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