Clinical Research Laboratory Information Management System Trials 
Cloudbyz
APRIL 30, 2023
Clinical trials are complex and time-consuming endeavors, requiring efficient management and coordination between various stakeholders. Comprehensive Solution: Cloudbyz’s unified clinical trial management solution covers the entire clinical trial lifecycle, from study planning to close-out.
Cloudbyz
AUGUST 26, 2024
The clinical research industry is in the midst of a digital revolution, with Clinical Trial Management Software (CTMS) at the forefront of this transformation. The Early Days: Legacy CTMS Systems In the early days of clinical research, managing trials was a manual, paper-based process.
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Cloudbyz
AUGUST 8, 2024
Effective clinical trial management 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.
Cloudbyz
JUNE 10, 2023
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. Let’s explore.
Cloudbyz
APRIL 16, 2023
Clinical trial management systems (CTMS) are software solutions designed to help manage clinical trials. They provide a range of tools for study management, including tracking patient recruitment, monitoring data, and managing study budgets.
Cloudbyz
JUNE 2, 2023
Electronic Data Capture (EDC) has revolutionized clinical research and pharmaceutical drug development. However, adopting this system requires a significant financial commitment. Initial Costs The initial costs of implementing an EDC system can be substantial, encompassing both direct and indirect expenses.
XTalks
DECEMBER 5, 2023
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. The processes do not simply involve receiving a sample, testing it and producing a result, he says.
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