E-Prudent

... Revolutionizing clinical trials

In our endeavour to speed up the process of clinical trials and make them cost effective while improving accuracy and transparency, we realised that work load of those who conduct trials [Project managers, Clinical Research Associates (CRAs)] gets extremely tedious with the limitations of distance (onsite physical monitoring), time, and communication. These limitations directly affect the decision making and trial performance consequently the quality of data generated. So, we came up with ‘Wise and Precise’e-Prudent that has revolutionised our clinical trials.

e-Prudent is a comprehensive e-platform for remote monitoring and Interactive Web Response System (IWRS).


So how does e-Prudent revolutionise clinical trials?

  • Randomisation, Subject Enrolment, Emergency Code Breaking
  • Complete overview of site performance
  • Study drug tracking and inventory management on the same platform
  • Maintains data integrity
  • Lowers trial costs by improved decision making
  • User friendly and custom built portal for research team to carry out predefined actions
  • 21 CFR part 11 validated system
  • Provides real time data to CRAs and project managers helping them make swift and informed decisions thereby mitigating risks.
  • Maintains data integrity
  • User friendly and custom built portal for research team to carry out predefined actions
  • Lowers trial costs by improved decision making
  • 21 CFR part 11 validated system

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