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  Home > Product & Solutions > iPharmaTrack
    iPharmaTrack
  It takes 12 years on average for an experimental drug to travel from the laboratory to the medicine chest. Only five in 5,000 compounds that enter preclinical testing will actually progress into human clinical trials, and of these five, only one is likely to be approved by the regulatory authorities.

Experts forecast that the cost of producing a successful drug could top $2 billion by 2010 unless the pharmaceutical industry can identify new and better ways to improve efficiency and effectiveness of drug discovery and clinical trials. Cost pressures are enormous, even on those drugs already in the pipeline. In today's high-paced world of drug development, each day a new drug is not on store shelves can mean $1 million or more in lost revenues.

DoubleBridge iPharmaTrack suite helps companies of all sizes stay on top of these intense business and regulatory demands. This suite of software products can accurately track regulatory requirements, automate business workflow, streamline the drug submission process, and speed up product to market time.

iPharmaTrack suite includes the following modules:

  • Regulatory Event & Activity Tracking (REAT)

    Pharmaceutical companies of all sizes face the daunting challenge of managing drug product submission, compliance, and tracking. These extensive multiple demands require automated solutions that supply users with real-time data that meet strict regulatory requirements. DoubleBridge Technologies, Inc. can help companies meet these challenges with a sophisticated Regulatory Activity Tracking (RAT) system developed after years of extensive field experience.

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  • Global Audit Acitity Tracking (GAAT)

    DoubleBridge's Global Audit Activity Tracking (GAAT) is a revolutionary audit activity tracking system comprised of an integrated set of web-based software tools that cover all aspects of quality management and audit tracking for pharmaceutical firms. This out-of-the-box solution includes modules for internal and vendor audit tracking with corrective and preventative action tracking built-in, as well as modules for submission document quality management, regulatory commitments, and change control.

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  • Global Regulatory Requirement Tracking (GRRT)

    The pharmaceutical industry is constantly being challenged to meet increasing regulatory requirements. These compliance regulations are extremely complex, change frequently and are difficult to monitor. The Regulatory Requirements Tracking system provides a secure, up-to-date library of country specific regulatory requirements and procedures, which can be used by multinational corporations.

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