RealTime Software Solutions has acquired Complion, bolstering the combined organization’s position as a leading provider of clinical research solutions.
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eReg for Sites and Site Networks

We partner with clinical research sites to deploy industry-leading solutions for real-time regulatory compliance, helping site teams to:

  1. Activate, train, and support investigators and study teams on demand
  2. Maintain monitor-ready regulatory or site files
  3. Effortlessly enable monitoring visits whether remote or onsite
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Start more trials and investigators, faster

Enable remote staffing, support, and monitoring

Boost productivity and profit; do more with less

Rapidly eliminate paper, redundancies, and manual processes

Ready to get started? Request a Demo

Ready to get started?
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Automate Regulatory Compliance

Complion’s unique compliance-automated platform helps remotely manage all stakeholders and documentation throughout the clinical trial life-cycle and your research portfolio – on demand.

Quickly Activate Study Team

During startup and throughout study conduct, activate investigators, clinicians, and study team members from any location in minutes with role-based automation of delegation, credentialing, training, and document availability.

Always Monitor Ready

Perfect site file organization with folders, keywords, and naming conventions that are always up to date within the ISF. Connect to shared documentation from your IRB, email, vendors, labs, facilities, sites, and more.

Self-Service Monitoring

Add monitors to specific studies on demand with role-based access by SOP - including for remote view-only source data review and verification - with self-service search, collaboration, and full reporting on monitor activities.

Regulatory Requirements

Ensure accurate completion of regulatory requirements with purpose-built workflows for delegation of responsibilities, safety letters, living logs, training, eSignatures, and more.

Site Networks (SMOs, IROs)

Increase profit and scale to more investigators and studies with fast startup and comprehensive support by providing visibility, option for central management, and effective use and collaboration with clinical site resources.

For research sites or coordinating centers running multi-center investigator-initiated trials as the sponsor and/or ARO/CRO, please see our Sponsor/CRO solutions page.

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Trust in Our Expertise & Focus

As the founder of the eReg market, we provide unmatched value and site-regulatory expertise, and we enable rapid and full adoption. As a best-of-breed provider, we can rapidly integrate across the ecosystem to all major site CTMS vendors, major cIRB / shared site platforms, and many sponsor / CRO solutions.

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"The Complion platform is well thought out and intuitive to use. On top of that, the team they have is absolutely stellar! Their team is receptive to feedback, and keeps in touch regularly to make sure things are going well. Their customer support is top-notch, too. I love working with them, and can't recommend this team / platform highly enough."
Brooke Barrick, BA, CCRP, Clinical Regulatory Specialist, J. Lewis Research Inc.
"As a CRA, it is invaluable to be able to review the ISF when I have time, to download documents for my TMF when necessary, without having to bother study staff. Excellent solution for CRAs."
Teresa, Senior CRA
"The service and knowledge of the implementation team and Complion support is top quality customer service."
Maria DiLorenzo, Research Regulatory Specialist, UCHealth
“During an FDA surveillance inspection, the inspector was able to collect the required regulatory documents in less than an hour with Complion. And the inspector had no findings.”
Susan Bonner, BS, RPh, Regulatory Manager, Tekton Research, Inc.
"Our enterprise level subscription gives us the ability to centralize documents and disseminate them accordingly. Furthermore, the team is very receptive to feedback when it comes to new product releases."
Julia Brenner, Clinical Research Financial & Regulatory Manager, Coastal Pediatric Research
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See Complion in action!  Request a 30-minute personalized demo and we’ll walk you through how we can deliver industry-leading investigator regulatory solutions for clinical trial sites, sponsors, and CROs.
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