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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 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 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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Recent News
News  02-Jun-10 White Paper from Premier Research Reviews how to Optimize Country Selection in Oncology Clinical Trials
News  28-Apr-10 White Paper from Premier Research Reviews Risk Evaluation and Mitigation Strategies (REMS) and the Impact on Opioid Analgesics
News  26-Apr-10 Premier Research Pediatric Experts Presented Poster at 2010 ACRP Conference
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Upcoming Events
Event  29-Aug-10 13th World Congress on Pain
Event  08-Oct-10 2010 ESMO Congress
Event  17-Nov-10 Partnerships in Clinical Trials
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