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...
10 Maguire Road
Lexington, MA 02421
Founded in 2004
Key Executives for Virtify, Inc.
Vice President of Strategic Partnerships
Director of Product Management for SCM Solutions
Senior Director of Sales for Mid-Atlantic
Compensation as of Fiscal Year 2014.
Virtify, Inc. Key Developments
Virtify Announces New Release of Virtify RIM to Add XEVMPD Functionality to its Regulatory Information Management Platform
Nov 4 14
Virtify announced the release of Virtify RIM 3.1. With this release, Virtify has added major new functionality to its regulatory information management platform to support management of xEVMPD information and required submissions to the EMA. Virtify RIM users can now utilize a rich set of xEVMPD features as part of a full regulatory information management implementation or as a separate product with a future upgrade path to a full RIM product suite. In addition, Version 3.1 provides a foundation within the Virtify RIM product to meet upcoming IDMP requirements that will be effective in 2016. Virtify RIM is a web based solution that enables regulatory professionals to keep up with the rapid changes in the regulatory environment while addressing efficiency imperatives. In contrast to other solutions, Virtify RIM integrates into the tools companies already use. By leveraging these existing tools, Virtify RIM makes it easy to build and maintain essential regulatory operations data, including product registrations. Virtify RIM streamlines the effort to provide a single source of truth for regulatory information and emphasizes ease of use and deployment in order to simplify daily tracking and recording tasks. It seamlessly tracks filing plans, correspondence, commitments, submissions and product changes throughout the product lifecycle. Virtify RIM 3.1 automatically aggregates submission and product change data to produce detailed product registrations, eliminating the need for manual maintenance of product registration records. By providing transparency into regulatory activities, users across the organization have easy access to the data they need to for quick, informed decision-making. By adding the new EVMPD module, Virtify RIM helps organizations preparing for the upcoming IDMP compliance requirements that will be put in place by 2016.
Virtify, Inc. Announces Clinical Trial Disclosure Solution Agreement with Virginia Commonwealth University
May 29 14
Virtify, Inc. announced Virginia Commonwealth University (VCU) has signed an enterprise-level contract for its Clinical Trial Registration & Results (CTRR) disclosure software. Virtify announced the Program for the Academic/Research marketplace through its partnership with Forte Research Systems, Inc. VCU will become part of a working group of academic/research institutions that will provide product feedback and utilize Virtify’s CTRR offering to fulfill their regulatory obligations by disclosing their clinical trial information to the National Institute of Health’s clinicaltrials.gov system. The system will be implemented by the Office of Research under the leadership of VCU’s Chief Research Information Officer, Dr. David Fenstermacher. 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 has extensive experience supporting life science clients in managing complex clinical trial disclosure and regulatory compliance. Virtify’s CTRR software, combined with Forte Research System’s OnCore CTMS, will offer academic/research institutions the most complete overall solution for managing compliance with regulatory reporting requirements.
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.
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