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Virtify Launches Virtify SCM, A New Clinical Content Management Solution for the Life Science Industry

 Virtify Launches Virtify SCM, A New Clinical Content Management Solution for
                          the Life Science Industry

Software Platform Improves Pharma Compliance, Productivity, Quality; Reduces
Risk and Costs

PR Newswire

BOSTON, June 24, 2013

BOSTON, June 24, 2013 /PRNewswire/ --  DIA Conference, Booth #1647 -- Virtify,
Inc., a leading innovator in content and regulatory information management
solutions for the life science industry, today 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.

(Logo: )

"Clinical and regulatory content contained in mandated documents are vital
assets, often supporting drug development for decades. Yet inefficient
management of clinical content can handicap the enterprise in the face of
changing markets and regulatory needs," said Satish Tadikonda, President and
CEO of Virtify, Inc. "Virtify SCM's seamless management of clinical
information results in competitive advantage for the life science company.
Virtify SCM evolves content management to a new level of ease and
sophistication, delivering near-term risk reduction and cost savings with
long-term improvements in operational efficiency."

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.

According to industry analyst firm IDC Health Insights, a new drug costs from
$800 million to $1.2 billion to bring to market, and a quarter of this cost is
content and regulatory requirements. Traditional document management
approaches slow processes and isolate data. This promotes inefficiencies and
risk in reporting, planning and regulatory affairs.

Benefits of Virtify SCM

Virtify SCM takes a new approach to managing clinical content to gain better
insight into clinical operations. Benefits of Virtify SCM include:

  o Boosts Efficiency with Content Library. Virtify SCM leverages company
    content in a secure, searchable library of linked core data components.
    Content users receive notification when any applicable content is updated.
    Current regulatory forms and processes are also maintained. This master
    control facilitates accuracy and accountability of content assets and
    their growth, while reducing infrastructure.
  o Reduces Time and Cost with Document Automation. Virtify SCM maximizes the
    reuse of core structured data and regulatory templates to build
    submission, labels and other documents on demand. Submission and
    electronic sign-off requirements are noted.
  o Enhances Collaboration with Parallel Authoring. The content management and
    collaboration tools enable authorized workers to collaborate with a
    document in real time to better manage complex, multi-submission
    compliance requirements.
  o Better Accountability with Content Tracking. Virtify SCM records
    variations from master content and tracks its evolution and lineage. All
    changes and sources are inventoried, and the document is tracked to the
    final submitted form.
  o Ease of Use - Work the Way You Want. SCM uses a Microsoft® Word paradigm
    so medical writers, regulatory affairs and labeling professionals do not
    have to change their work flow and style practice. Rapid implementation is
    complemented by flexible delivery via subscription or perpetual licenses,
    in-house or using hosted systems.
  o Business Intelligence. Virtify SCM provides a unified view into the
    clinical content workflow with actionable, standard or custom reports and
    analytics to support clinical, regulatory or executive inquiries and
    audits. Such analytics result in a more agile enterprise.

A demo of Virtify SCM is available at DIA 2013, Booth #1647, Boston, MA, June
24-26, 2013.  A detailed Virtify SCM fact sheet is available at

The Virtify SCM software platform is complementary to related Virtify
solutions: 1) Virtify RIM:
Regulatory Information Management software to track and manage complex global
regulatory data and processes. 2) Virtify CTRR: Clinical Trials Disclosure
software to streamline and automate the mandatory clinical trial registration
and results disclosure obligations to the National Institute of Health and
other registries.

About Virtify

Virtify is the leading innovator in content and regulatory information
management solutions for life sciences. Many of the world's leading
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 life
science domain expertise has been leveraged by such companies as
Genzyme/Sanofi, Novartis, Pfizer/Wyeth, Regeneron, academic research centers
and CROs.  Virtify's easy-to-use software suite is the industry's only
solution to provide a secure, collaborative, web-based environment for
managing regulated content throughout the entire continuum – from pre-clinical
through product registration to commercialization. Visit us at

SOURCE Virtify, Inc.

Contact: Eric Meyers, Virtify, Inc., 617-301-8710,
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