Virtify announces the availability of Virtx eCTD version 2.7, a state-of-the-art web-based application for Electronic Common Technical Document Standard

Cambridge, MA - 14 April, 2008: Virtify is pleased to announce the release of version 2.7, a comprehensive solution for compiling, reviewing, and submitting Applications to Life Sciences Regulatory Agencies using the Electronic Common Technical Document standard.

This release builds upon version 2.6 with the following new features and benefits by supporting submissions to EU regulatory agencies including all the features and benefits available in previous releases for FDA Submissions.

The web based architecture of the virtx:eCTD solutions provides a multi-user environment for users to work on different parts of a submission concurrently. The solution provides the status of documents at different phases of the submission with appropriate icons, alerts and notifications.

About Virtify

Virtify is a global company, with headquarters in Cambridge, MA and other international locations in India, Philippines and Bulgaria. We use cutting edge web-based technologies and global delivery capabilities to develop and implement innovative software products and solutions for the Life Sciences industry.

One of our strengths is our deep domain knowledge and demonstrated leadership in emerging global standards. Virtify is one of the first companies to introduce a pure web-based Structured Product Labeling (SPL) solution for managing the entire life cycle of labels. Virtify was the first to submit a SPL demo to the Food and Drug Administration (FDA) and the first company to submit a Regulated Product Submission (RPS) drug device and combination drug submission to the FDA. The first RPS Viewer was also introduced by Virtify we were the first to submit an Electronic Common Technical Documents (eCTD) drug and device submission to the FDA. In addition, we have recently been the first to submit messages in emerging standards such as eStability and ICSR. Such leadership on standards has enabled us to work closely with clients in effectively planning for emerging standards while addressing current mandates and standards for clinical and regulatory submissions.

Virtify’s clients include several pharmaceutical, and biotechnology companies, and its projects have spanned the R&D lifecycle, from discovery through commercialization.. For additional information about Virtify, please visit
http://www.virtify.com.