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The Business Need for Clinical Trial Management Systems

Life Sciences Review | Tuesday, November 30, 2021
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Clinical Trial Management Systems (CTMSs) are extremely valuable for analyzing trial timetables and budgeting, especially when trials are on the critical path.


FREMONT, CA: Clinical trial management was made more convenient owing to CTMSs. All organizational data, tracking information, and reporting may now be accessed from a single, dependable location. This cuts down on the amount of time, effort, and resources needed to run a trial. As a result, there has been a trend among pharmaceutical and biotechnology firms to reduce the number of employees required, resulting in a smaller enterprise. The CTMS enables timely reporting and data exports if it is kept up to date as the study advances.


Since the early 2000s, when electronic systems became better connected, clinical trial management has required far less manual labor. The usage of CTMSs minimizes the number of persons required to enter data, lowering the risk of human mistakes. Before CTMSs, one of the key issues was a lack of consistency between data sources. 


Since the deployment of CTMSs, this has been removed or greatly reduced. Having all of the clinical trial data in one location is easier and more dependable. For audits and health authority inspections, this provides credible documentation and confirmation of trial oversight and administration.


CTMSs have a wide range of applications in clinical trial management. Country and site status, monitoring reports, deadlines, and trial preparation are all common uses. Having a centralized system for all monitoring reports, approvals, action items, and observations is quite beneficial. This makes it simple to generate reports and do trending studies to determine where problems may exist.


Management should watch the status of clinical trial programs involving 10-20 distinct trials, especially to see if milestones are being reached. CTMSs are extremely valuable for analyzing trial timetables and budgeting, especially when trials are on the critical path. By putting this in an electronic system, management can focus on a specific trial state or look at data from a more holistic program perspective.


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