Quality Integrated monitoring: Setting new standards for the next decade of clinical trial practice
2011
Integrated Monitoring in Clinical Trials
publication
Author Information
Author(s): Kamala Rai
Primary Institution: Novartis Healthcare Pvt. Ltd.
Hypothesis
How can integrated monitoring improve clinical trial practices?
Conclusion
Integrated monitoring can enhance the efficiency and effectiveness of clinical trial management.
Supporting Evidence
- The global clinical research market requires contracting with 95,000 clinical trial sites and recruiting approximately 1,200,000 patients annually.
- The role of the field monitor is being redefined to improve efficiency and reduce costs.
- Integrated monitoring can lead to better collaboration and communication between trial sites and sponsors.
Takeaway
This study talks about how clinical trial monitors can work better by using new methods to keep track of studies, making it easier to help patients and researchers.
Methodology
The article discusses the evolving role of clinical trial monitors and the adoption of integrated monitoring practices.
Digital Object Identifier (DOI)
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