A Review: Virtual Clinical Trials

A Review: Virtual Clinical Trials

Authors

  • Zainab Hussain Department of Pharmaceutical Chemistry, Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telangana
  • Farheen Fatima Department of Pharmaceutical Chemistry, Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telangana
  • Arfah Fatima Department of Pharmaceutical Chemistry, Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telangana
  • Ausaf Butool Department of Pharmaceutical Chemistry, Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telangana
  • Anupama Koneru Department of Pharmaceutical Chemistry, Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telangana

Keywords:

Virtual Clinical trials, digital technology, data collection and management, regulatory compliance.

Abstract

Virtual clinical trials allude to clinical trials that take advantage of digital technologies, including computer and mobile device apps, web-based tools, and remote monitoring devices, for one or more of the trial processes, such as participant recruitment, informed consent, counselling, measurement of endpoints, and adverse event monitoring, to prevent or lessen the need for participant visits to the trial site. The advantages of such trials may comprise higher recruitment rates, lower dropout rates, better compliance, reduction in time for trial completion, and lower costs. The use of such trials elevated multitudinous during the COVID-19 pandemic and is likely to continue in the future.

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Published

2026-01-07

How to Cite

Zainab Hussain, Farheen Fatima, Arfah Fatima, Ausaf Butool, & Anupama Koneru. (2026). A Review: Virtual Clinical Trials. International Journal of Pharmacy and Analytical Research, 15(1), 17–22. Retrieved from https://ijpar.com/ijpar/article/view/1041