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
Electronic Clinical Trial Requirements
RABIT Trial Features
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: