On the path to trial success, compliance, efficiency and innovation are everything

Wingspan Regulated Content Management solutions from IQVIA are a proactive approach to managing the increase in digital content for trials. We help you make your users more efficient by automating processes and reducing steps so you can collaborate more effectively with your partners. Streamlined processes support all your global locations while at the same time helping you comply with the requirements of Health Authorities worldwide. 

Be on top of your documentation, aligned with sponsors and CROs, and ready for successful Health Authority inspections. 

  • Spend less time on admin functions and reduce the burden of managing sites.
  • Get experienced help and advice to manage planning, maintenance, monitoring, and archiving of your regulated content with solutions that reduce hassles and errors associated with outdated paper record-keeping and filing processes. 
  • Improve relationships between sponsors and contract research organizations through automatic document delivery, filing, submissions, and reporting.

From solutions for small CROs and biotechs without marketed products to support for Top 10 Pharma, IQVIA can offer an easier way to improve productivity, compliance, and collaboration — even when budgets are tight.

Find out more about how Wingspan Regulated Content Management solutions from IQVIA can help your trial succeed.

Electronic Trial Master File Software
Ensure the safety of your patients and integrity of your trial results with a complete, consistent and compliant Trial Master File.
Submission Document Management
Streamline creation, approval and organization of submission-ready content.
SiteZone Clinical Site Document Exchange
Administration and documentation can be overwhelming. Especially when a study involves dozens of sites — or even hundreds of sites.