Clinical Trial Safety
Improve Data Quality and Investigator Satisfaction
 Sentrx SafetyTrak® Clinical Trial Safety centralizes and standardizes the collection of serious adverse events (SAEs) across multiple clinical trials, multiple protocols and multiple CROs around the world. Our Safety Response Center is staffed with experienced healthcare professionals to receive phone calls and faxes from investigators reporting SAEs.
Because we focus on obtaining high quality data through active query with investigators, SafetyTrak® Clinical Trial Safety reduces the amount of inquiries generated from each case and the time each query remains unresolved. StudyTrak™ Reporter, a module of the SafetyTrak® Technology Suite, provides a structured and standardized tool to collect SAEs and manage adverse event cases.
SafetyTrak® Clinical Trial Safety enables each SAE to be assessed quickly and accurately to determine if it meets the criteria for a 7-day expedited report or suspected unexpected serious adverse event (SUSAR) report. It also increases visibility into potential safety signals during clinical trials, when the opportunity exists to proactively examine the issue. For more information, download these documents:
| SafetyTrak® Clinical Brochure |
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| SafetyTrak® Clinical Case Study |
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Drug Safety in Clinical Trials
DIA Today, June 2006
© Drug Information Association, 2006 |
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