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Services » Clinical Functional Services » Adaptive Clinical Trials Design » Overview

MaxisIT is all set to help its clients to eliminate the late stage disorders most possibly occurring in a clinical trial due to small percentage of error mostly in the phase II set up of a clinical trial as it is impossible to counter the late stage disorders in a trial or a accounting for the time, money and efforts spent on the study.

MaxisIT with all of its experience and expertise realizes adaptive clinical trial designs are highly effective than traditional procedures in cases where arises uncertainty surrounding the dose, effect size and variability, clinical endpoint or patient populations. MaxisIT predicts a high percentage of growth in Adaptive Clinical Trials Design in the near future and is ready to be a pioneer in this area.

MaxisIT believes its adaptive clinical trials design services are very promising as they aim to advance a decision to the Client at the very early stage in a clinical trial about the error or disorder which may be likely to occur in the future course of study. It gives the client an option to continue, rectify or terminate the study along with the first hand information of the possible error in the latter stage of clinical trials in a single source view.

MaxisIT has an end to end Clinical Trials Product called CT Renaissance™ which has various modules which caters from the protocol design, Study design to Submission of the clinical trials to a regulatory authority. As a part of these solutions MaxisIT has a separate Statistical module which takes care of these Adaptive Clinical Trials with a detailed expertise on the following features:

  • Adjusting Randomization Probabilities
  • Linking Randomization Systems and Drug Supplies Tracking
  • Bringing live information from various sources (EDC) to one real time system for detailed analysis
  • Efficient Electronic Data Capture capabilities for the entire study for future reference
  • Adaptive Analysis
  • Interim Analysis Capabilities
  • Forecasting and Predictive Analysis Capabilities
  • Rules Engine Supporting Scheduling of Interim Analysis
  • Efficient Statistical Analysis Capabilities
  • Adaptive Explorer Supporting Single Source View of one or more studies providing cross-functional reports

This module for Adaptive Clinical Trials is also available as a separate sevices for the clients in the portfolio of MaxisIT Clinical Functional Services. MaxisIT through this service offering ensures that Adaptive Clinical Trials Design, Analysis and Execution is made simple as MaxisIT can take care of clients Adaptive Clinical Trials Design and Adaptive Clinical Trials Implementation as well.

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A major pharmaceutical organization accomplishes FDA eSubmissions with the help of MaxisIT.

MaxisIT standardizes clinical trial systems for a large pharmaceutical organization with the help of CDISC data standard models.


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I recommended that our IT and Operations groups partner with MaxisITInc because they are an independent company that can function as an advisor to our organization. Their experiences and capabilities allow them to act as a translator and trainer between Information Technology and our business units.


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Contact our Services Specialist at our Corporate Headquarters in Metuchen, NJ.

MaxisIT Inc.
203 Main Street,
Metuchen, NJ-08840
Ph.732-494-2005


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