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news roundup
Quintiles and DaVita Clinical Research have allied to provide capabilities and solutions for renal disease clinical trials.
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Unlock the full potential of RBM using this new framework which integrates EDC with advanced RBM tools and goes beyond identifying risk to enable immediate action!
 Listen to this podcast to learn how
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The KMR Group has completed its industry analysis on the comprehensive cost of clinical trials.
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Simplifying the complexities of global rare disease drug development
Live Webinar: Thursday, September 15 at 11:00 EDT
 Register now
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The European Medicines Agency (EMA) has published a final report about its pilot project on adaptive pathways, which it describes as a product development concept for medicines that address patients' unmet medical needs.
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 Click here to watch a short video about Covance's Xcellerate Informatics platform, an innovative 4-module solution to optimize the planning and execution of clinical trials.
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Transforming Patient Recruitment through Patient and Site Engagement
Live Webinar: Tuesday, August 23, 2016 at 11 am – 12 noon EDT
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Articles
Sponsor executives reported that their companies had made carefully-considered decisions about the functional competencies that would be retained in-house.
The Avoca Group's Quality Consortium held its fifth annual Summit with over 250 attendees from over 50 companies whose discussions brought out unifying themes around innovation and patient centricity.
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Blog Posts
Industry experts shared their knowledge on running high quality, small budget clinical trials covering clinical operations to clinical data management and biostatistics.
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mHealth
Virtual clinical trials represent a relatively new method of collecting safety and efficacy data from clinical trial participants, from study start-up through execution to follow-up.
Adam Amdur, Chief Patient Officer of the Sleep Apnea Association launched the SleepHealth mobile app study, the first large-scale observational sleep study that leverages mobile health to collect real world data.
Limited use of “Bring Your Own Device,” or BYOD, in regulatory studies to date is mainly due to industry concerns spanning two areas.
This article surveys several pressing regulatory topics that clinical trial researchers need to consider when using mHealth technologies, including good clinical practice (GCP), fitness of use, security/privacy, electronic records (and eSource data), researcher oversight, and inspection preparedness.
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