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Clinical trials are complex and time-consuming endeavors, requiring efficient management and coordination between various stakeholders. Cloudbyz’s Unified Clinical TrialManagement Solution, built on the Salesforce platform, offers a comprehensive, customizable, and secure platform for streamlining clinical trial operations.
21 CFR Part 11 is a crucial component of regulatory compliance in clinical trials and, more broadly, any industry subject to the regulations of the U.S. This blog post will serve as a comprehensive guide to understanding and implementing 21 CFR Part 11 compliance in your clinical trials. Food and Drug Administration (FDA).
Effective clinical trialmanagement requires seamless integration with various systems and technologies, as well as robust data management and security protocols. This blog will highlight the integration capabilities of Cloudbyz EDC and provide best practices for managing and securing clinical trial data.
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Central labs ensure consistency in test methodologies, equipment and reporting standards, which is vital for the integrity of clinical trials. Accurate and reliable lab data play a crucial role in any clinical trial. There’s an entire ecosystem in the central lab and in a clinical trial that you need to be aware of,” he says.
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