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Preliminary Product Assessment
Clinical Trials Management
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IVRS: Clinical Logistics and Tracking
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Experienced and well-trained clinical trial managers and CRAs are key to the successful implementation of Phase I-IV clinical trials. Westat's rigorous staff training and comprehensive SOPs ensure that all aspects of clinical trial implementation are managed effectively. Our project managers and CRAs maintain open, continuous, and documented communications with clients, clinical sites, investigators, and regulatory authorities to ensure timely and accurate dissemination of vital information.

Services:

  • Site identification, qualification, and selection
  • Protocol and informed consent development
  • Case report form development
  • Organization of investigator meetings
  • Site training
  • GCP and GLP auditing
  • Clinical site monitoring
  • Monitoring of analytical laboratories
  • Pharmacy auditing
  • QA/QC oversight
  • Preparation of interim and final study reports
 
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