SPOTLIGHT
Virtify invites you to a virtual roundtable on “Addressing the EMA EVMPD Mandate: Insights from pharmaceutical company executives”scheduled for Wednesday, 25th January 2012 10AM EST.
Click here to register
Virtify EVMPD Software and EVMPD Compliance Services provide flexible, cost effective options for meeting July EU deadline for new EVMPD data.
Compliance In Control
Virtify helps life sciences companies gain control over their entire compliance life cycle. Our Structured Content Management products dramatically increase efficiency and flexibility, while improving content quality and accuracy.
Virtify named as one of the "Cool Vendors in Life Sciences, 2010" by Steven Lefebure and Dale Hagemeyer of Gartner.
Events
Upcoming Webinar
“Addressing the EMA EVMPD Mandate", Pharmaceutical company executives discuss steps they are taking to comply with this mandate.
Jan. 25, 2012 10AM EST
Click here to register.
Recorded Webinar
Teden Consulting and Virtify presented a Global Disclosure Webinar "Managing Global Registeries for Clinical Trial Disclosure: Challenges and Resolution".
Watch the recorded webinar here!
News
- January 23, 2012
Roundtable of Industry Experts to Discuss Impact, Implications of EVMPD Mandate. Read More - December 15, 2011
Virtify Launches New EVMPD Product and Services. Read More - October 19, 2011
Virtify Launches European Module for Global Labeling. Read More - September 13, 2011
Virtify Launches Clinical Trials Registry-India (CTR-I) Module. Read More - June 29, 2011
Virtify secures $5.5 M in Series B Financing. Read More