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Virtify Delivers SaaS Clinical Trial Disclosure Solution for Mid-Market Life Sciences Companies
Date:9/9/2009

encies. With its SaaS-based delivery, the Virtx CTRR solution is also able to maintain compliance with all new and emerging regulatory mandates, reducing risk, and insulating business users from the complexity of changing compliance requirements. At the same time, life sciences companies can maintain complete control of their clinical trial disclosure processes - just as they would with an in-house software solution - but at a fraction of the overall cost of ownership.

"Clinical trial sponsors of all sizes must take stock of their existing business processes and systems to ensure that accurate and compliant communication of clinical trial data is available in the public domain," said Dr. Satish Tadikonda, president and founder of Virtify. "Our SaaS-based CTRR solution enables life sciences companies of all sizes to address this challenge by managing the entire clinical trial disclosure life cycle more efficiently and cost-effectively."

Virtify's Virtx Clinical Trial Registry & Results Solution - Key Features and Capabilities

  • Collaborative, web-based environment for managing clinical trial disclosure
  • Complete lifecycle management of the disclosure process from internal review, through approvals, postings, and results maintenance
  • Ease-of-use and intuitive interface promoting greater user adoption
  • Internal workflow management and automation for improved processes and quality
  • External workflow management with regulatory agencies for improved accuracy and consistency
  • Unique submissions comparison/reconciliation feature for greater speed and efficiency
  • Up-to-date compliance with current & emerging global regulations and standards:
  • US FDA, WHO, FDAAA, CTRI, EMEA, and other authorities
  • Compliant with FDA 21 CFR and SAE/AE reporting
  • Robust validation, auditing, secu
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SOURCE Virtify, Inc.
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