Toronto, Canada (PRWEB) June 19, 2014
In the early stages of a clinical study, getting off to the right start is critical. Yet, up to 70% of clinical trials experience study start up delays, and almost half are completed late. Each day a timeline slips can keep new products from patients and put millions in future revenue at risk.
The highest levels of efficiency can be realized by implementing experienced-based and mutually agreed-upon site identification and selection strategies, by leveraging customized templates, processes and technologies, and by leveraging a highly dedicated regulatory start-up team. This will accelerate the study start-up process, reaching the goal of sites initiated and ready for enrollment as quickly as possible.
The speakers will discuss how they are using an industry-leading approach, supporting sponsors with Fair Market Value (FMV) compensation analysis to ensure compliance with Anti-Bribery/Anti-Corruption (ABAC) compliance. They will demonstrate how the following strategies, processes, and technology help maximize productivity and reduce cycle times.
For more information or to register for this webinar, visit: Accelerated Start-Up: The Right Start to Trial Success.
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