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In designing clinical trial studies, data and process management is challenging. RABIT is a simple, user-friendly, and efficient solution for implementing clinical trials in compliance with international standards. In the RABIT, in addition to generating random and anonymous codes based on a variety of randomization patterns (to ensure the correct implementation of the randomization, concealment, and blinding process), various roles have been considered for data entry, monitoring, and data management.

Advantages of Conducting Clinical Trials Electronically

RABIT advantages in designing clinical trial studies
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Cost-effectiveness

By eliminating additional processes in clinical trials and converting them to electronic, the cost of implementation is greatly reduced.

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Increased Data Quality

Increase the quality of recorded data by using new and user-friendly tools in designing electronic forms in clinical trials and applying simple rules.

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Tracking Processes

Manage and track processes better by using the comprehensive management panel for clinical trials in RABIT.

Electronic Clinical Trial Requirements

Some of the requirements mentioned in the CFR 21-Part 11 document in electronic health data capturing that have been systematically implemented in RABIT Trial.
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Data Security

Any recorded data that is changed in the system is easily traceable as to who, when, and what variable was changed. This feature, which is known as Auditing in clinical trial studies, causes all the changes in your study to be recorded.

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Data Management

Including maintaining the confidentiality of patient data through encryption, encryption of all information exchanged between the client and the server, defining different access levels for users, preparing a backup file of project information on the server on a daily basis

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Data Quality

Using tools available in the RABIT Registry form builder, you can apply any type of validation to your variables. Using hundreds of predefined variable types will help you design your forms faster.

RABIT Trial Features

Create your own account now to view RABIT Trial full features.
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Manage and monitor data during the data gathering process

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No dependency on programming and data science team

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Access level per eCRF and action (add, edit, and view)

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Design eCRF in a user-friendly environment

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Online/offline mobile application

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Dynamic reports and data export

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Dictionaries for drugs, diseases, etc

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Events logs in the system

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Data encryption in database

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Multi-center studies

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Randomization algorithms

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Inclusion and exclusion criteria

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Comprehensive dashboards

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Follow up phases

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Patients electronic health record

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Sound record of interview process

Some of Clinical Trial Studies Designed In RABIT

We have had the experience of designing several large clinical trials in collaboration with universities and major pharmaceutical companies in the world, and we have investigated various aspects of the design of such studies in software systems. The Polly Pill drug study in collaboration with Oxford University or Metformin in collaboration with Merk made us understand all the software standards for conducting a clinical trial study according to CFR 11-Part 21 and implement this experience in the form of software modules in the RABIT. Some of the clinical trial projects carried out in Rabit are:

  • COVID-19 Vaccine Clinical Trial System - Barkat Pharmaceutical Group
  • COVID-19 Vaccine Clinical Trial System - Pasteur Institute of Iran
  • Scorpion Sting Clinical Trial
  • Remdesivir Clinical Trial
  • Botox clinical trial
  • Somatin clinical trial