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For pharmaceutical organizations, compliance with 21 CFR Part 11 (Part 11) is essential when using software solutions that store and maintain electronic records and electronic signatures. Part 11, issued by the U.S. Food and Drug Administration (FDA), establishes the requirements for ensuring that electronic records are trustworthy, reliable, and equivalent to paper records. Visit - https://www.slingshotpharma.co....m/blog/fda-computer-

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