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The Leading eRegulatory Solution for High-Performing Clinical Research Sites, Sponsors, and CROs. Complion’s platform is the accepted standard built specifically for clinical researchers. Our solution ensures the highest level of compliance with the greatest efficiency and the least amount of work. Allowing you to focus on what really matters ...
https://complion.com/contact/
https://complion.com/roi/
Source: CenterWatch-Complion study, 2020; N= 202 research sites. Average months from study startup to database lock = 24 months, estimated 255.5 hours of staff time for regulatory-related tasks per single clinical trial, Fair Market Value for CRC or Regulatory Specialist estimated at $50.00/hour.
https://complion.com/overview/
Overview - Complion. Imagine all your regulatory documents organized in one place, accessible from. wherever you are while maintaining the highest level of security. As requirements expand and clinical trials grow more complex, it becomes increasingly more difficult to manage regulatory documentation. The Complion platform helps research sites ...
https://www.glassdoor.com/Overview/Working-at-Complion-EI_IE1046450.11,19.htm
Complion, the leading eRegulatory provider for sites, was founded by certified clinical research professionals to empower sites. In collaboration with leading sites and based on best practices, Complion developed Acuvia, a common standard platform for sites to store...
https://complion.com/resources/
Complion is committed to advancing the clinical research community through education and technology. Please enjoy our free educational resources. LOGIN Call us anytime: 1-800-615-9077
https://www.bloomberg.com/profile/company/1697098D:US
Complion Inc. operates as a software company. The Company develops and provides a web based document and workflow management platform for clinical research sites and their sponsors.
https://complion.com/sponsors-cros/
Sponsors and CROs that work with sites using Complion see increased quality through accurate submissions, improved TMF quality, completeness, and timeliness. They also gain real-time access to all site files from one location with a single password. By achieving site utilization, Sponsors and CROs achieve their goals of increased quality, cost ...
https://complion.com/3-requirements-for-a-remote-sdr-sdv-solution/
Fortunately, there is a very simple solution if the right eRegulatory solution is used. Here are the three primary requirements when looking for a remote source document review solution: 1) HIPAA Compliance – This should be top of mind. Confirm with the eRegulatory solution provider the platform complies with the provisions of the HIPAA ...
https://www.sec.gov/Archives/edgar/data/1581876/000158187615000003/xslFormDX01/primary_doc.xml
Name of Issuer; COMPLION INC. Street Address 1 Street Address 2; 1621 EUCLID AVE. SUITE 1251: City State/Province/Country ZIP/PostalCode Phone Number of Issuer
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