Trial Tracking System

Our client, has a network of 3,000 professionals located in the U.S., Canada, Europe and Puerto Rico.  It was challenging for the client to track the trials/samples since the research was being conducted at various sites. Also, randomized clinical trials were distributed across the investigators.

We have developed a windows-based application, Trial Tracking System to administer the clinical trials and protocols. It includes creating and planning the trial, mapping locations, members, sites, investigators with the trial. The system manages and maintains the trials with improved positive impact on the quality of the data.  It helps to achieve sustainability by controlling the spiralling costs of escalated clinical trials.


  • To start a clinical trial, the Principal Investigator completes the form and sends it to the sponsors (NSABP). The sponsor will incorporate this information with technical data into an IND (Investigational New Drug Application) and send it to FDA (Food and Drug Administrator). Once the FDA approves, these sponsors will inform the Investigators to start the Clinical trial.
  • The application is capable of tracking all the data entered in the forms by multiple investigators (i.e. Principal-Investigator, Sub- Investigator)
  • The Co-Investigators are authorized by Principal-Investigator
  • Every Co-Investigator who is participating in the trial need to sign form and this should be approved by FDA