Knowledge Center
Valuable insight, readily available.
Virtify is committed to serving as a valued source of information and insight for life sciences regulatory compliance professionals. Our thought leadership encompasses every aspect of regulatory content management—from the development of new technology standards to strategies and best practices that advance the practice of compliance in a rapidly evolving global regulatory landscape.
We hope you find the content provided in this resource valuable to your own work. Check back often, as new content is posted periodically.
Openly Accessible Content:
Product Data Sheets
- Virtify® RIM Global Regulatory Business Intelligence Product Sheet
- Virtify® SCM Clinical Structured Content Management Product Sheet
- Virtify® SCM Global Labeling Innovation via Structured Content Management Product Sheet
- Virtify® SPL Virtify’s SPL Product and Outsourcing Services Product Sheet
- Virtify® CTRR Global Clinical Trial Disclosure Product Sheet
- Virtify® EVMPD Product Sheet
Case Studies
- Transparency/ Disclosure Compliance
- Regulatory Compliance
- Clinical/ Regulatory Compliance
- Lab Optimization
- Research Informatics
- Commercialization
Recorded Events
- VIRTUAL ROUNDTABLE on Addressing the EMA EVMPD Mandate where pharmaceutical company executives discussed the steps they are taking to comply with this mandate.
The Roundtable Report can be downloaded here.- Moderator:
Dr. Andrew Marr, Managing Director of Marr Consultancy Limited
Panelists:
John W Kiser, Senior Director, Regulatory Operations, Abbott Laboratories, USA
DrJörgLautz, Head of Application Management Group, Global Regulatory Affairs, Grünenthal GmbH, Germany
Gordon Topping, Associate Director, Information Strategy, Takeda Global R&D Centre (Europe) Ltd, UK
RichardEddershaw, Director, Regulatory Informatics, Global Regulatory Affairs, GlaxoSmithKline R&D, UK
- Moderator:
Registration Required:
White Papers and Articles
- Six Pillars: Factors to consider in selecting a Clinical Trial Disclosure SystemThis article originally appeared in the March 2011 issue of Regulatory Affairs Pharma (www.regulatoryaffairspharma.com)
- Process Assessment and Improvement Approach
- Effective Tools for Efficient Operations:
Key Considerations for the Ideal Mix of Tools and Complementary Processes to Enable Optimal Operations in Your Organization - Maximize Productivity with Limited Resources:
How Virtify can help extend your capabilities or support critical functions - Transform Your Organization with Effective Planning and Reporting:
How Virtify applications can help your organization formulate a roadmap for effectively managing the influx of standards, and plan your resources and activities. - Effective Strategies to Manage Costs in the Changing Global Regulatory Environment
- Virtify Platform: A Standards-based, Integrated, Scalable Platform for Managing Submissions Over the Internet
