Virtify Webinar Alert: 'The Moving Target of Global Clinical Data Disclosure' Presented by FiercePharma

Jun 23, 2010, 16:05 ET from Virtify, Inc.

CAMBRIDGE, Mass., June 23 /PRNewswire/ --

What: Virtify, Inc., the market leader in enterprise content compliance (ECC) solutions, will co-host the webinar, "The Moving Target of Global Clinical Data Disclosure." As the focus on clinical trial disclosure intensifies under evolving global regulations, life sciences companies are required to disclose increasing amounts of trial information for public consumption. In order to satisfy the demand for transparency, what steps must you take and when? What constitutes full regulatory compliance? What technology solutions are available today to streamline and reduce risk? This webinar will provide expert perspectives on the global clinical trial disclosure challenges facing regulatory affairs and compliance executives, and how to effectively navigate the vagaries of communicating clinical trial activities and results to regulators worldwide.

Who:

  • Hosted: George Miller, Editor, FierceBiotech IT
  • Speaker: Henrietta Ukwu, M.D., Senior Vice President, Global Regulatory Affairs
  • Speaker: Patricia Teden, Principal, Teden Consulting LLC
  • Speaker: Steve Selfors, Manager, Commercial Operations, Virtify, Inc.

Why Attend:  Learn the essential considerations for global clinical trial disclosure and the technology solutions that can expedite compliance and reduce total cost of submissions.

When: Thursday, June 24 at 2:00 pm ET / 11:00 am PT

Where: Register online or visit www.virtify.com  

About Virtify

Virtify is the market leader in Enterprise Content Compliance software solutions for life sciences. Organizations rely on Virtify solutions to reduce time-to-market, risk, and cost by managing and automating the complex regulatory compliance and content exchange requirements throughout the product life cycle. 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. The company plays a leadership role in the development of global regulatory standards and is an active participant in a variety of standards committees. Virtify's software products combined with comprehensive professional services and deep domain expertise enhance quality and compliance for some of the world's leading life sciences companies. Located on the Web at www.virtify.com

SOURCE Virtify, Inc.



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