Products - Virtify

By: Virtify  09-12-2011
Keywords: Content Management, life sciences, Clinical Trials

Accelerating product pipelines are driving the need to create, approve and disseminate regulatory content faster and more efficiently, with total accuracy. Meeting those challenges means replacing inefficient serial processes with structured content management (SCM) solutions that enable parallel processes and content re-use.

Virtify products make it easy to achieve the full productivity potential of structured content management. Our content-centric approach enables you to:

  • Dramatically accelerate workflows with parallel content processes.
  • Improve quality and accuracy by re-using approved, validated content.
  • Keep pace with changing regulations and business rules, automatically.
  • Manage all content creation activities more effectively and more efficiently.
  • Get up and running quickly with turnkey, off-the-shelf, enterprise products.

Virtify SCM Framework

Our products are built on an open, extensible, web-based architecture that uses common, XML-based infrastructure and business components to deliver a unique combination of advantages:

  • Component-based parallel authoring, reviewing and approval, with robust versioning.
  • Content re-use and linking across documents, with automated change notification.
  • Comprehensive, centralized workflow management with event triggers.
  • Library of re-usable XML content components generated automatically.
  • Automated “injection” of new rules and requirements.
  • Flexible metadata management, with the ability to easily configure metadata fields.

Built specifically for the life sciences industry, Virtify products provide a complete solution for improving your content creation and management processes—from clinical trials disclosure to product labeling submissions to medical writing & submissions.

Keywords: Clinical Trials, Content Management, life sciences

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Other products and services from Virtify

09-12-2011

Structured Content Management - Virtify

Component-based structured content management system that dramatically increases efficiency through content re-use and parallel authoring—enabling seamless collaboration among authors and reviewers located anywhere in the world. Behind every life sciences product stands a mountain of written content: clinical studies, reports, clinical protocol development materials, manufacturing SOPs, marketing materials.


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Clinical Trial Disclosure - Virtify

Virtify helps you address all of these challenges with a unified, web-based, commercial-off-the-shelf software product that enables you to comply with clinical trials disclosure regulations with unsurpassed efficiency, consistency and predictability. To enhance public awareness and safety, regulatory agencies around the world are dramatically expanding requirements for public disclosure of clinical trials information and results.


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Medical Writing & Submissions - Virtify

Component-based structured content management system that dramatically increases efficiency through content re-use and parallel authoring—enabling seamless collaboration among authors and reviewers located anywhere in the world.


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Solutions - Virtify

Virtify solutions dramatically increase speed and productivity, while improving content quality and accuracy. Web-based environment for managing regulated content throughout the compliance continuum. At Virtify, we understand the challenges you face every day.


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Labeling - Virtify

Many life sciences companies are implementing global labeling solutions to manage labeling content and submission, for FDA's SPL standard in the U.S. and to meet requirements under EU 726/2004 Article 57in Europe. Life sciences companies marketing products in multiple countries face even greater challenges, including keeping pace with evolving standards for multiple jurisdictions and maintaining overall consistency.


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Virtify European Labeling - Virtify

Virtify European Labelling is the only off-the-shelf product that improves and streamlines XML-based product information submissions in a collaborative, web-based structured content management environment. It provides centralized product information lifecycle management with integrated workflow, including content creation, review, approval, translations, and bidirectional communication with EMA.