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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 130 Phase 2–4 trials conducted throughout North America, Europe, South Africa, Asia, and Australia. Our IXRS group includes a strong, stable team of developers and support personnel that have extensive experience with all facets of IXRS, including Schedule II and Schedule III substances. We offer our IXRS as part of a full service offering or as a standalone service.

Features of our IVRS include:
  • 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 include:
  • 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

ezRand
In additional to our traditional platform, we also offerezRand. This IWR system provides clients with a rapidly deployed, cost effective solution for performing automated randomization, subject tracking, study medication dispensing, and clinical supplies management. This system is built upon our robust IWRS platform and is comprised of a comprehensive suite of commonly used modules. Each module can be configured via 'data-driven' parameters drastically reducing costs and timelines.

Case Studies
Case Study  Real-Time Access to Study Data
Case Study  Managing Clinical Supplies in a Global Trial
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Upcoming Events
Event  14-Apr-10 19th Annual Partnerships in Clinical Trials Conference
Event  21-Apr-10 Informa's Clinical Evaluations & Investigations for Medical Devices
Event  23-Apr-10 ACRP 2010 Global Conference & Exhibition
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