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The issue of reporting bias is well-known and non-publication of clinical trial results is unfortunately common. Various initiatives have been implemented to remedy this issue such as the FDA Amendments act in September 2007, which requires submission of results to a publicly accessible database within 12 months of study completion. However, this act only applies to a subset of Phase II-IV trials and not all clinical research.
To build and maintain gold-standard, next generation R&D intelligence tools, Sitetrove, Trialtrove, Pharmaprojects, and Trialpredict have been undergoing a major program of investment. In addition to the many new and exciting changes on the horizon, the robust and reliable Citeline tools that you use to inform your business decisions will formally join Informa’s Pharma Intelligence family of brands.