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The Choice, Not Chance: How to Mitigate the Risk of Selecting a Non-Enrolling Site for your Clinical Trial webinar was presented to you by Sitetrove and Trialtrove, both part of the Informa Pharma Intelligence family of tools.
The industry’s most accurate and comprehensive investigator and site intelligence solution, at Sitetrove, a team of expert analysts scour over 40,000 public sources to bring you the latest vital information on the global clinical trial landscape, with content tailored to specific therapeutic areas. Trialtrove is the industry’s leading authority for accurate, current and comprehensive clinical trials intelligence, providing a deep understanding of the clinical landscape in your focused areas of research, supported by expert therapeutic area analysts.
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Pharmaprojects: track pharma R&D
Gain vital insight into study feasibility, site selection, and investigator prioritization with granular data from the new Informa Pharma Intelligence Patient Proximity API. Protect yourself against costly trial delays by using it to choose the right investigators with relevant and sizable patient proximity.
Medtech Insight: global medical technology news & analysis
By Sue Darcey
Bioresearchers at the Centers for Disease Control and Prevention are hoping that diagnostic platforms previously used to develop tests for outbreaks of other epidemic respiratory diseases, including SARS and MERS, can be built on to develop new diagnostics to detect more cases in the current coronavirus outbreak, US infectious disease authorities say. This comes as more patients are monitored around the US for the disease, and a Chicago woman returning from China tests positive.
Topics Drug approval Clinical Trials Coronavirus Policy and regulation
Medtech Insight: global medical technology news & analysis
By Sue Darcey
The US Food and Drug Administration (FDA) stands poised to proceed with hastened approvals for 2019-coronavirus (nCoV) diagnostics, treatments and vaccines, if a public health emergency is declared, after an infected US traveler who caught the disease in Wuhan, China returned from the province to Washington State. Spread of the disease has reached a crisis level in China, and the World Health Organization met on 22 and 23 January to consider what actions to take to contain the virus, while issuing an interim laboratory test guidance for use in diagnosing the disease.
Topics Drug approval Clinical Trials Coronavirus Policy and regulation
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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.
The industry’s most trusted drug development database, Citeline's Pharmaprojects has been covering pharma R&D across global markets for 35+ years. With 68,000+ drug profiles including 15,000 drugs in active development, it’s the go-to resource for preclinical, clinical, and pipeline coverage, and lifecycle management tracking.
Trialtrove is the go-to resource for clinical trial research. Easily track your competitors' clinical R&D activity with expert insights and continually monitored trials.
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