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Virtify Announces Webinars on Regulatory Information Management Strategies for the Life Science Industry



Virtify Announces Webinars on Regulatory Information Management Strategies for
                          the Life Science Industry

Understanding and Implementing Regulatory Information Management (RIM) for
Small and Mid-Sized Life Science Companies

PR Newswire

LEXINGTON, Mass., Nov. 14, 2013

LEXINGTON, Mass., Nov. 14, 2013 /PRNewswire/ -- Virtify, Inc., a leading
innovator in content and regulatory information management solutions for the
life science industry, today announced a complementary Webinar series on
regulatory information management (RIM) for small and mid-sized life science
companies on Tuesday, Nov. 19, 2:00 pm EST, and Dec. 10, 1:00 pm EST. To
register please visit http://www.virtify.com/news-events/events/.

(Logo: http://photos.prnewswire.com/prnh/20110131/NE38689LOGO )

The webinar is a two-part series designed to help regulatory professionals
understand what RIM is, the ongoing value that can be extracted from good RIM
processes and how to start a RIM initiative.  Virtify CEO Dr. Satish Tadikonda
and Product Manager Bernie Coney will offer practical, experience-based advice
and share best practices for keeping your RIM approach simple, yet impactful.

Part 1:  What is Regulatory Information Management and Why Should You Care?
Date:  Tuesday, November 19, 2013
Time:  2:00 PM EST

Presenters in this webinar will provide practical advice on regulatory
information management for growing companies while answering the following
questions:

  o What is RIM?
  o When does the current pipeline warrant a new look at RIM?
  o Why should my team be concerned with RIM (and how do we get value from
    it)?
  o What are current approaches (pros and cons) and best practices for RIM?
  o How do we scope and prioritize our RIM requirements?

Part 2:  Developing a Simple, Cost-Effective Approach to RIM
Date:  Tuesday, December 10, 2013
Time:  1:00 PM EST

Presenters will discuss the development of a framework for initiating a RIM
project, how to determine and document a projected ROI and how to leverage
quick wins upon implementation. Among the learning objectives are:

  o How and where do I start a RIM project?
  o How can I design the initiative to show the quickest wins while still
    keeping the project simple and cost-effective?
  o How can I best use ROI to support the RIM project goals?
  o How will this project impact current workloads and resources?

Who Should Attend?
These webinars are designed to help regulatory professionals in small and
mid-sized companies understand RIM. Roles that will find value in this event
include:

  o VP or Director of Regulatory Affairs/Regulatory Operations
  o Manager of Regulatory Affair/Regulatory Operations/CMC
  o Regulatory Information and Regulatory Informatics Managers
  o Dossier and Registration Manager
  o Regulatory IT Liaison

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
http://www.virtify.com.

SOURCE Virtify, Inc.

Website: http://www.virtify.com
Contact: Eric Meyers, Virtify, Inc., 617-301-8710, emeyers@virtify.com
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