Our Services: IVRS/IWRS

​Premier Research provides a reliable, fully validated, 21 CFR Part 11 compliant Interactive Voice/Web Response System (IVRS/IWRS) including ePRO capabilities that allows our clients to automate many aspects of their trials with added flexibility and confidence. Regardless of complexity, scale and duration of a study, Premier Research’s technology can be utilized to increase efficiency in your clinical trial.

Premier Research has employed our IVRS system in more than 200 Phase I-IV trials conducted throughout North America, Europe, South Africa, Asia, and Australia. Our IVRS/IWRS group includes a strong, stable team of developers and support personnel that have extensive experience with all facets of IVRS/IWRS, including Schedule II and Schedule III substances. We offer our IVRS/IWRS as part of a full service offering or as a standalone service.

Features of our IVRS/IWRS +
  • Patient Randomization made simple for the investigator whether centralized, stratified, or adaptive algorithms
  • Clinical Supply Management provides study coordinators and the team with improved drug accountability and expiry information allowing for less drug wastage and cost control
  • Patient Diary Collection offers improved compliance, data accuracy, and availability of patient diary data
  • Visit Tracking eliminates the need for paper based enrollment logs and allows oversight of patient enrollment by project team to prevent over-enrollment
System Highlights+
  • 24/7 multilingual capability and support
  • Data exports and customized reporting available via secure internet connection Use of robust, scalable technology allowing for timely development of protocols
  • Flexible system allowing for adaptive design
  • Full business continuity plans and disaster recovery plans in place ensuring maximum system availability

Knowing what works, sharing what we know. It's what we do. Best.