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Virtify, Inc. Delivers Industry's First Enterprise Content Compliance Software Suite for Life Sciences Companies

ting ICH as well as regional standards
  • Virtx CTDS - Clinical Trial Disclosure System for global compliance automation and management
  • Upcoming Standards Support:
    • Virtx PIM - Labeling supporting EU EMEA Product Information Management standards
    • Virtx RPS - Product supporting HL7 (Health Level 7) Regulated Product Submission standards
    • Virtx eStability - Product supporting HL7 Electronic Drug Stability standards

  • Enterprise eCompliance Products

    • Virtx SCM - Workflow enabled structured content management for collaborative document authoring, reviewing, assembly, publishing, and delivery
    • Virtx CDS - Product for managing a company's Core Data Sheet including change notifications and response tracking
    • Virtx RIS - Information Exchange Platform combining process, methodology and a modular, componentized platform for organizational-specific R&D and commercialization information
    • Virtx RMA - Web-based Resource Management and tracking
    • Virtx ST - Submissions Tracking and planning
    • Virtx IDM - Investigator clinical trials management
    • Virtx PRS - Patient Registry/clinical trial management

    Virtify is a featured solution provider at the DIA Annual Meeting Booth 403.

    About Virtify

    Virtify is the market leader in Enterprise Content Compliance solutions for life sciences. Organizations rely on Virtify solutions to reduce time-to-market, risk, and costs by managing and automating the complex regulatory compliance and content exchange requirements throughout the product life cycle. Virtify's easy-to-use Virtx software suite is the industry's only solution to provide a secure, collaborative web-based environment fo

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