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MaxisIT’s eDefine™ software solution under the CT Renaissance™ enterprise suite offers a multitude of functionalities, making it a one-stop-solution for both your software and services needs. MaxisIT has extensive breadth and depth of Define.xml. Our Define.xml group evaluates the trials in the design phase in order to create an efficient validation management process to ensure a timely service which is within budget and of top quality. 
Features - Easy and intuitive web-based software for faster, more efficient SDTM validation & Define.xml generation
- Web-based, wizard driven, point-n-click reports development
- Built-in repository of statistical methods, standard reports ‘templates and shells.
- End-to-end traceability of data & referential linking
- Comprehensive metadata management
- Enables efficient decision making by quick implementation of emerging data standards
- Low total cost of ownership (TCO)
- Interoperable and can be fully integrated with other systems
- Round the clock support
- GCP-ICH & 21 CFR Part 11 complaint processes and software infrastructure
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| Success Stories |
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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.
MaxisIT derives successful implementation of a web-based
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| Press Releases |
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MaxisIT recognized for eAdaptive – innovative solution within clinical trials and research category METUCHEN, NJ – April 29, 2010 – CHI’s Bio-IT World Confer
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| Product Contact |
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Contact our Services Specialist at our Corporate Headquarters in Metuchen, NJ.
MaxisIT Inc.
203 Main Street,
Metuchen, NJ-08840
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| CT Renaissance |
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| Clinical FSP |
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Site Specifications
