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MaxisIT  

 Product Awards

 


 White Papers
Adaptive mid-course correction via cross-functional monitoring and decision-making

Imputing ISO8601 dates from character variables containing partial dates

A scalable platform for clinical trials - Interoperability and automation in a web-based environment

A Relational Understanding of SDTM Tables


Products » eCollabora

CT Renaissance™ eCollabora™, is a user friendly web-based collaborative medical writing, reviewing, clinical trial disclosure and tracking system. Our centralized system allows Writers and Reviewers to communicate instantly irrespective of their global location. Writer content and reviewer comments are stored in a centralized repository and internal versioning is maintained for the same. Our system provides a  user-friendly interface and editor to help Writers and Reviewers streamline collaborative clinical trial protocol writing processes.

eCollabora

Our internal workflow system allows users to track the internal process from start to finish. Web-based collaborative review and authoring solution offers a secure, structured and controlled review environment and is unique such that the review takes place in the browser - there are no documents to download. It is designed for a secure, real-time review process with a strong audit trail and traceability.

Features

  • Role-based secured user management
  • User dashboard
  • Business process workflow
  • Web-based editor support
  • Collaborative authoring
  • Collaborative reviewing
  • Clinical trial disclosure
  • Review comments
  • Standardized yet customizable templates
  • Fail-safe
  • Audit trial and traceability
  • Version controlled deliverables
  • Document formats support
  • Alerts and email notification
  • Intuitive reports
  • 21 CFR part 11 compliance
  • Web based and user friendly THIN client interface
  • Optimized performance

 Customers




 Success Stories

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


 Press Releases
MaxisIT recognized for eAdaptive – innovative solution within clinical trials and research category
 
METUCHEN, NJ – April 29, 2010 – CHI’s Bio-IT World Confer

 Product Contact

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

MaxisIT Inc.
203 Main Street,
Metuchen, NJ-08840




 CT Renaissance

eCollabora

eRoI

eNsure

eDefine

eAnalyze

eProfile

eSUBMIT




 Clinical FSP

Clinical Data Management

Biostatistics and SAS Services

CDISC and Regulatory Services

Documents Management

Collaborative Medical Writing

Electronic Submission (eCTD)




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