InForm GTM

 

InForm GTM - A Complete Solution for Global Clinical Trials

The Phase Forward InForm Global Trial Management (GTM) platform, with its intuitive user interface, multi-language capabilities and associated software modules, delivers a robust solution to meet the needs of today’s global EDC user.  Its flexible and scalable architecture and user-friendly design accommodate the needs of smaller organizations looking for solutions today that will expand to meet their needs tomorrow.

 The InForm GTM platform provides comprehensive data entry, edit-checking and query management functionality for data capture and data cleaning.  Designed with the needs of global studies in mind, InForm GTM utilizes the same feature set for users around the globe, minimizing training and support costs. The InForm GTM solution offers the flexibility to run a multi-language study with the advantages of a single underlying database architecture. 


The product’s robust reporting and analysis capabilities provide real-time visibility and access to trial data. With earlier and more insightful views into trial data, sponsors can make more informed decisions, mitigating risks and improving overall trial conduct.

 

The InForm GTM product’s supporting modules encompass trial set up and design, trial conduct, standards-based document archive and submission, and integration with third-party clinical and non-clinical software solutions.  Systems such as IVRS, CTMS, Imaging and ePRO can easily integrate with the InForm environment through the support of Web Services and industry standards.  Modules for randomization and trial supply management (Clarix), study design (Central Designer), and medical coding and dictionary management (Central Coding) can be added – to provide a comprehensive eCDM solution.

The InForm GTM platform and its supporting modules are designed to provide clinical sites and trial sponsors with all the tools required to efficiently conduct and manage EDC-based clinical trials.

  • Central Designer streamlines the study build process by reducing setup and validation time, allowing study teams to work in parallel, and enabling companies to apply industry standards

        

  • Central Coding facilitates multi-study, industry-standard and customized coding of drug names, indications and adverse events

        

  • InForm Portal provides a communication vehicle for site and sponsor information exchange and document management with version control capabilities

        

  • Auto Site Assessment (ASA) is a Web-based service offering for assessing a site’s hardware compatibility for participation in an InForm trial

        

  • User Management Tool (UMT) is a Web-based service offering for provisioning sites and users within an InForm trial

        

  • Phase Forward IRT provides randomization and trial supply management via interactive response technology

        

  • InForm CRF Submit generates electronic common technical document (eCTD) compliant Adobe® Portable Document Format (PDF) editions of the InForm electronic case report forms (eCRFs) for site and sponsor archive and eSubmission to regulatory agencies

        

  • InForm Adapter provides a number of Web services-based interfaces that enable integration, extensibility and workflow across the InForm modules and with other third-party software systems

        

  • InForm Reporting and Analysis leverages a built-in reporting model that enables a sponsor’s staff to run both standard and ad hoc operational and clinical reports

        

  • WebSDM is a data validation and review tool for tabulation data submitted in CDISC SDTM standard format used to pre-validate submissions and CRO data, providing a submissions data mart with FDA-compatible review tools
  
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