Deviation management is an essential principle under Good Manufacturing Practice (GMP) regulations and standards. It refers to the proper disposition of products or processes that don’t conform to approved specifications.
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Deviation management software automates manual quality processes and facilitates compliance with GMP regulations that require formal deviation control such as 21 CFR Part 211 for pharmaceutical companies and 21 CFR Part 820 for medical device firms. More and more life sciences and other regulated companies rely on deviation management software to digitize their quality processes for compliance purposes.