1.0Solutions BPAhttps://www.bpa-solutions.net/frHow to Make Your Quality System CFR 21 Part 11 Compliant - BPA Solutionsrich600338<blockquote class="wp-embedded-content" data-secret="QRIezAPMqO"><a href="https://www.bpa-solutions.net/fr/cfr-21-quality-system/">Comment rendre votre système qualité conforme à la norme CFR 21 Part 11</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://www.bpa-solutions.net/fr/cfr-21-quality-system/embed/#?secret=QRIezAPMqO" width="600" height="338" title="« How to Make Your Quality System CFR 21 Part 11 Compliant » — BPA Solutions" data-secret="QRIezAPMqO" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript">
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</script>https://www.bpa-solutions.net/wp-content/uploads/2017/08/bf1.jpg495135In this article we will discuss major CFR 21 part 11 requirements. We will present how an Office/SharePoint-based quality management system complies with relevant regulations for the life science industry. People who use systems to create, modify, maintain, or transmit electronic records shall employ procedures and controls designed to ensure the authenticity, integrity, and the […]