When: |
30 Mar through 30 Mar 2017 | |
Where: |
Online Event | United States | |
Website URL: |
https://www.atozcompliance.com/trainings-webinar/life-sciences/clinical-research/remote-monitoring-to-improve-clinical-trial-quality/danielle-delucy/300183?utm_source=ref&utm_medium=30Mar | |
Sponsoring organization: |
AtoZ Compliance | |
Categories: |
Medicine & Health - Medical-Speciality |
Keywords:
Event description:
Strategies for remote monitoring, review of data for trends & how to make the most of risk based monitoring
Across the industry, companies are striving to find ways to improve operational efficiencies. Currently, over 80% of site-based documentation today is still fully paper based, with both cost and risk consequences for the entire clinical trial process. Specific liabilities of a paper-based system include audit and inspection risk, reduced site productivity, manual reconciliation of TMF and site records, as well as the lack of visibility into site performance.
Strategies for saving time and money, without compromising oversight and quality, are an ongoing challenge within the industry. In an age where technology is ever present from ordering medications online, consulting with a physician, and having “live” conversations in chat rooms about medical issues, the clinical research industry has been slow to maximize the use of technology.
Posting date:
23 February 2017 | 138 views
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