news roundup
According to the results of a new ‘State of eConsent’ survey released by CRF Health, 55% of respondents’ organizations will adopt eConsent in 2017, rising to 82% by 2020.
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Designed exclusively for Clinical Development, by Clinical Development experts - The industry’s first training and educational portal filled with white papers, thought leadership articles, and much more all at your fingertips!
CTA: Dive into Almac Clinical University
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IAOCR, an accrediting organization for international clinical research, is spearheading an emergency summit to discuss how to safeguard the clinical research industry in the U.K. before and after Brexit. It will take place on Wednesday, April 5th at a venue in the South Bucks/Berkshire area.
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Clinical Trials, Technology and Transformation
Acquire insights from 70+ influential industry leaders touching on technology innovation, mHealth, patient-centricity, effective collaborations, reducing costs and more at T3: Trials, Tech and Transformation, May 11-12, 2017 in Orlando, FL. Act now as early registration rate deadline is March 17th. Want more incentive? Save an additional $250 off current rate. Use Code: T3ACT.
 Click here for further details |
CHDR and OmniComm will collaborate in a new technology evaluation center in Leiden, the Netherlands, where innovative products and electronic data capture (EDC) management systems will be immediately tested in an onsite clinical setting.
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IRT EUROPE – Interactive Response Technologies in Clinical Trials
4-5 April 2017 | Hilton Paddington | London, England
Leverage IRT to Enable Innovative, Flexible and Efficient Supply Chain Management for Clinical Trials
 www.cbinet.com/irteu |
The latest updates to people moves and business news.
The survey will evaluate how endpoint adjudication is impacting study design, and uncover operational challenges with endpoint adjudication and endpoint adjudication outcomes.
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Improving Clinical Trial Transparency, Collaboration and Efficiencies
Live Webinar: Wednesday, March 29 at 11:00am EDT
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Use Challenge Trials Effectively in Clinical Studies: Lessons Learned from H3N2 Influenza Virus
Live Webinar: Tuesday, March 28 at 3 pm CEST and Thursday, April 6 at 10 am EDT
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Are Local IRBs Really Necessary?
On Demand
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Articles
Through economies of scale and mechanisms enabling clients to provision and decommission a variety of virtual computer, storage, and networking resources on demand, these cloud platforms are able to provide an alternative to the traditional data center that can be significantly less expensive.
Companies that fail to implement predictive modeling solutions that analyze data to determine the probability of achieving their target outcome when making their site selection decisions are at risk of falling behind their industry peers.
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Blog Posts
As a former FDA official and resident fellow at the conservative American Enterprise Institute (AEI), who also has strong ties to pharma, Scott Gottlieb was the clear choice of industry, as well as many research and patient groups.
Let’s take the conservative view: assuming your organization is conducting 20 or more trials per year, shortening the timeline of each trial in your clinical development pipeline by one week could add up to more than $1 million in savings. |
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