In addition to our excellent IT services, DoubleBridge is firmly established in industry focused, cutting edge software products and solutions for Pharmaceutical clients. These products and solutions include:

• ROSETTA eCTD Suite

  Four independent, integrated eCTD software applications for the creation, validation, viewing, and archiving of eCTD submissions.

  • ROSETTA phoenix: eCTD view
  • ROSETTA scribe: eCTD publish
  • ROSETTA sceptre: eCTD validate
  • ROSETTA pyramid: eCTD archive
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• OrniPoint SharePoint Suite

  OrniPoint SharePoint suite is a web-based, off the shelf solutions/tool kit that will address all the challenges faced with content management in regulated industries. Completely integrated with SharePoint framework, OrniPoint SharePoint suite lowers your total cost and maximizes your benefit. OrniPoint SharePoint suite guarantees less transition time from implementation to business as usual..

  • OrniPoint Branta, the SharePoint Virtual Document Manager
  • OrniPoint King, the SharePoint Document Relationship Manager
  • OrniPoint Griffin, the SharePoint to Documentum Connector
  • OrniPoint Tern, the SharePoint Migration Tool
  • OrniPoint Falcon, the SharePoint Regulatory Content Management System
  • OrniPoint Nest, the SharePoint Regulatory Content Archival System
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• iPharmaTrack

  Out-of-the-box, web-based software tools for quality management, audit tracking, regulatory submissions and change control for pharmaceutical companies.

  • Regulatory Activity Tracking System
  • Compliance Audit Tracking System
  • Global Regularly Requirement Tracking System
  • Regulatory Submission Tracking, Archiving and Retrieving System
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• GCTT® System

  Clinical Trial is a multi-phase, high cost, high risk and high return on investment, if successful, operation conducted globally around the world. Drug sponsors, medical experts and clinical trial planners are often frustrated of not knowing how many patients have participated in the trial, how they are treated and where and how many medications are needed. Global Clinical Trial Tracking (GCTT?System) uses multi-channel interactive messaging technology (MCIMT) leveraging text messaging services, instant messaging services, email and fax services, interactive voice by phone and interactive web technologies. It provides the complete clinical trial patient treatment tracking and drug supply logistical support services that is critical component of global clinical research program. GCTT?System automates patient enrollment, randomization, medication assignment, just-in-time clinical supply inventory management with real time clinical study reporting dashboard. GCTT?System is your partnership towards a faster, more cost effective and high quality clinical trial to bring new drug to market.

  Your Benefits
  
  GCTT?system enables partnership with clients to benefit from the following:

  • Patient Screening/Enrollmment and Randomization
  • Dynamic Dose Calculation
  • Guaranteed study blindness for speedy regulatory approval
  • Real-time Site/Depot Inventory Tracking Management & cost saving
  • Real time global clinical study status dashboard reporting
  • In-house 24x7x365 Global Technical Support
  • Multi-lingual capabilities
  • Real time Integration with CTMS, EDC, DSMS
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