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Sterility testing plays a vital role in pharmaceutical quality assurance by verifying that products are free from viable microbial contamination. While traditional methods, such as those outlined in USP <71>, have been the industry standard for decades, they are often slow and come with certain limitations.
This article explores advancements in rapid sterility testing, including ATP (adenosine triphosphate)-based technologies and how these innovations can enhance regulatory compliance, improve efficiency, and increase testing accuracy.
Download now to learn more about the regulatory landscape, upcoming compendial updates, advantages and limitations of ATP-based testing, and the future of sterility testing.