Home Services Experience Client Comments Work Ethics Contact Useful Links	Services in Clinical Trial Management CRF Completion Instruction   We provide full service in clinical trial management. Our clinical operation group consists of experienced clinicians and site monitors, follows ICH guidelines for Good Clinical Practice in conducting trials, and provides professional outcomes in clinical trial data collection and review. Investigator Selection and Grant Management   Patient Enrollment Tracking   Study Initiation, Monitoring, and Close-out Visits   CRF Review and Data Query Resolution   Adverse Event, Medication, and Disease Terminology Coding   Safety Monitoring and Serious Adverse Event Report Tracking     Other services: Trial Design   Trial Management   Data Management   Medical Writing   Statistics & SAS Programming   Pharmacoeconomics
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