Health Care Technology
Company Overview of Virtify, Inc.
Virtify, Inc. provides structured content management software solutions for life sciences companies. It offers Virtify European Labeling, an off-the-shelf product that improves and streamlines XML-based product information submissions in a Web-based structured content management environment; EudraVigilance Medicinal Product Dictionary (EVMPD) that helps companies to comply with the European Union’s EVMPD legislation; and Virtify SPL Module that enables users to create SPL submissions in a Web-based structured content management environment. The company also provides Virtify Core Data Sheet, which enables users to centralize, streamline, and organize the management and dissemination of core s...
55 Cambridge Parkway
Cambridge, MA 02142
Founded in 2004
Key Executives for Virtify, Inc.
General Manager of Philippines Operations
General Manager of Indian Operations
Compensation as of Fiscal Year 2013.
Virtify, Inc. Key Developments
Indiana University Contracts with Virtify, Inc. for Clinical Trial Disclosure Solutions
Aug 19 13
Virtify, Inc. announced Indiana University has signed an enterprise-level contract for its Clinical Trial Registration & Results (CTRR) disclosure software. Indiana University will utilize Virtify's CTRR to fulfill their regulatory obligations by disclosing their clinical trial information to the National Institute of Health's clinicaltrials.gov system. The system is funded and being implemented by the Indiana Clinical and Translational Sciences Institute (CTSI), Purdue University and the University of Notre Dame funded by the National Institutes of Health. Virtify's CTRR streamlines and automates the mandatory registration and clinical results disclosure obligations to the National Institute of Health and other registries. It provides a compliance view across all clinical studies, allowing for better reporting, proactive compliance and patient safety. Virtify CTRR is architected for change. Its unique XML Rules Injection technology is designed to provide the speed and flexibility needed to meet all global disclosure requirements while minimizing the overhead and complexity of change management.
Sarah Cannon Research Institute Signs an Enterprise-Level Contract with Virtify, Inc. for its Clinical Trial Registration & Results Disclosure Software
Jul 15 13
Virtify, Inc. announced that Sarah Cannon Research Institute has signed an enterprise-level contract for its Clinical Trial Registration & Results (CTRR) disclosure software. SCRI will utilize Virtify's CTRR to disclose their clinical trial information to the National Institute of Health's clinicaltrials.gov system as mandated by federal regulation. The old paradigm for managing disclosure throughout the clinical trial process has changed, including at academic and research organizations. Many now recognize that the large number of disparate, investigator-driven studies at these institutions, coupled with constant updates to these studies and increasingly complex disclosure requirements, render manual processes too cumbersome and error-prone. Virtify's CTRR software helps streamline and automate the mandatory registration and results disclosure postings to the clinicaltrials.gov website and to other registries. The software also has the ability to provide a compliance view across all studies at an institution, allowing for better reporting and proactive compliance. Virtify's CTRR software offers academic/research institutions the most complete overall solution for managing compliance with regulatory reporting requirements including supporting integrations to "Off the Shelf" or custom applications.
Virtify, Inc. Releases Virtify SCM, New Software Platform for Creation, Reuse and Tracking of Clinical and Regulatory Content
Jun 24 13
Virtify, Inc. announced the release of Virtify SCM, a new software platform for creation, reuse and tracking of clinical and regulatory content. Virtify SCM (Structured Content Management) takes an asset management approach to improve collaboration and enables the automation of documents used throughout the drug product life cycle – from pre-clinical through product registration to commercialization. Virtify SCM improves compliance, productivity and quality while reducing risk across the drug product portfolio. Virtify SCM is a secure, collaborative, Web-based environment for managing regulated content through linked data components that automate and track all information known about a product, trial or objective at all stages of the development. Virtify SCM uses business rules-based templates and builds a library of re-useable content. It leverages organizational data across all operations, including R&D, submissions, labeling and marketing. Virtify SCM makes global regulatory compliance more routine, maximizing resources and producing more and better products in less time.
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February 26, 2013