Drive better decisions faster with real-time data at your fingertips.

Our technology innovations target rapidly evolving clinical trial models, in support of virtual trial data collection, IRT, RTSM, remote monitoring, eCOA/ePRO, reporting, communication, registries, and real world data collection platforms.

ePRO for Clinical Trials - IVR Clinical Concepts (IVRCC)
User-Friendly ePRO
Clinical Trial Material Management - IVR Clinical Concepts
Real-Time Clinical Trial Material Management
Subject Screening, Registration and Randomization - IVR Clinical Concepts
Subject Screening, Registration & Randomization
E-Clinical Integration - IVR Clinical Concepts
Seamless E-Clinical Integration
Patient Recruitment and Outreach - IVR Clinical Concepts
Patient Recruitment
E-Clinical Integration - IVR Clinical Concepts
Chart Reviews

We work with top 10 Pharma companies, large academic institutions, innovative specialty biotechnology companies, large and small CROs, medical device companies, commercial service companies, healthcare groups, Oncology consortia, and EDC technology providers around the globe. Our application is highly scalable and able to accommodate small individual site IIT studies to large multi-national trials with unlimited numbers of sites, subjects, and modalities, with varying complexities.

  • Pharmaceutical Companies
  • Biotechnology Developers
  • Medical Device Firms
  • EDC Vendors
  • Contract Research Organizations
Testimonial
Testimonial

Therapeutic Areas - IVR Clinical ConceptsIVR Clinical Concepts has deployed subject registration, randomization, trial supply management (RTSM) and ePRO/eCOA clinical services for numerous global projects and studies in multiple Therapeutic Areas.

How we’re different:

  • With 30 years of experience, we have deep knowledge of data collection.

    We’re adept at addressing unique clinical trial technology challenges across many therapeutic areas.

  • We think outside the clinical trial box.

    We build custom applications without the custom cost. Our flexible platform delivers technology solutions to solve your data problems at any budget.

  • We’re all about the experience.

    We bring the trial to patients with decentralized clinical trials, ePRO/eCOA, and BYOD to achieve high compliance from subjects. Our dedicated team continuously monitors and supports your study, from IVRCC build to close-out.

  • We’re dedicated to QA.

    Our dedicated QA department stays on top of validation procedures, regulatory compliance, and all quality assurance factors to verify data security, privacy and integrity.

  • Real-time data means real-time decision making.

    Having real-time study knowledge at your fingertips gives you the ability to adapt and adjust, increasing trial speed and reducing trial cost.

  • Our service doesn’t end at launch

    Our dedicated team of professionals is always available with 24/7/365 support to ensure all needs are met quickly and completely from start to finish.

Get Started

  • 1

    Get in touch – call us or send us a message

  • 2

    We’ll create a proposal based on your needs

  • 3

    We’ll work together to solve your clinical trial challenges
    and implement technology solutions to optimize your trial

Contact Us
Schedule a Demo of Clinical Trial IVR, IWR, ePRO and IRT solutions - IVRCC