Benefits of integrated clinical trials systems in risk based monitoring

Authors

  • Mohammed Saleem Khan Department of Risk Based Monitoring, Tata Consultancy Services, Mumbai, Maharashtra, India
  • Bharat Kumar Shukla Department of Risk Based Monitoring, Tata Consultancy Services, Mumbai, Maharashtra, India
  • Veerbhadra Nayak Department of Risk Based Monitoring, Tata Consultancy Services, Mumbai, Maharashtra, India

DOI:

https://doi.org/10.18203/2349-3259.ijct20161411

Keywords:

Data integration, Risk based monitoring, Clinical trials, Clinical trial systems, CTMS, Leaner integration, Cross functional integration, Data quality, Data coding, Issue management, Risk management, Trends, Patterns, Clinical site, Adap

Abstract

In the global world of integrated system, most industry recognized system integration is critical for optimal use to generate globally acceptable data, even clinical research industry is going through a paradigm shift from use of traditional system to integrated system to enhance the data availability on real time and supplements faster review and reporting of critical data points. But altogether to achieve 100% system integration, we need to create all compatible system with each other which require less mapping of different databases with reduced low data migration time.

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References

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Published

2016-05-09

How to Cite

Khan, M. S., Shukla, B. K., & Nayak, V. (2016). Benefits of integrated clinical trials systems in risk based monitoring. International Journal of Clinical Trials, 3(2), 55–58. https://doi.org/10.18203/2349-3259.ijct20161411

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Section

Review Articles