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3rd Annual Innovations in Clinical Data Management Conference



 
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Product Code: 2290
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About the Product
Includes presentation materials from the conference. Presentations slides are in PDF. format. All files are available for immediate download.


About the 3rd Annual Innovations in Clinical Data Management Conference:

Ensuring the Appropriate Balance of Risk-Based Monitoring in Clinical Studies to Minimize Data Error & Maximize Regulatory Certainty, Updating Strategies to Meet Adaptive Trial Design, & Leveraging Technology to Increase Speed & Accuracy while Reducing Costs & Providing Clear Return on Investment

In a continued effort to reduce the overall length and cost of clinical research studies across the life sciences industry, many corporations look to clinical data management teams to find efficiencies in data collection and analysis to increase regulatory certainty, while reducing the length of studies. Implementation of risk-based monitoring, while supported by many in the industry, comes with an additional set of challenges for clinical data managers as sites are evaluated and risks measured, but can provide tremendous time and cost savings. Working with clinical teams on adaptive trial design studies has also proven successful as corporations look for more rapid results and earlier detection, but at the same time proves challenging for clinical data managers as inputs and protocols more frequently change.

As the industry continues to evolve and technology increasingly plays a pivotal role in clinical research studies, data managers are looking to implement robust standards for data collection, many of which are in line with CDISC standards. The increasing use of e-Source data will also be discussed, as executives debate the importance and efficiency of this format, but also the regulatory hurdles in validating and gaining oversight support when utilizing technology for ePRO or via mobile source documentation. Throughout the 3rd Annual Innovations in Clinical Data Management conference, presenters highlight success stories in working both internally as well as with external partners to ultimately meet the goal of streamlined clinical studies that meet robust data standards, achieving regulatory goals.


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