As health and life sciences industries continue to shift from paper to digital, CFR 21 Part 11, a regulation issued by the U.S. Food and Drug Administration (FDA), has become a cornerstone of compliant electronic recordkeeping. It defines how organizations must manage electronic records and signatures to ensure they are as trustworthy, reliable, and legally valid as their paper counterparts.
Compliance is essential for any organization using electronic systems in FDA-regulated environments, such as:
In this webinar, we break down the essentials of CFR 21 Part 11, including:
Michael Henry
VP, Growth Strategy | Drummond
Michael Zgourovski
Risk Assessor | Drummond
Payers, providers, and health IT developers share the drivers, challenges, and practices that are shaping interoperability testing today.
Meet one-on-one with a Drummond cybersecurity expert to discuss your current risks, security gaps, or compliance needs and receive a customized ACTION PLAN.
