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MAR.21/2017


news roundup

CRF Health Releases eConsent Survey Results

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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Monitor Temperature-Sensitive Logistics and Reduce Excursions
New InTemp by Onset is a seamless, end-to-end temperature monitoring solution for the storage and transportation of temperature-sensitive products throughout the pharmaceutical supply chain. Together, the InTemp data logger, mobile app, and cloud-based data warehousing platform reduce excursions by providing accurate, secure, and actionable temperature data through the point-of-delivery.
Learn more


Special Session in EU Over Brexit

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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Is Your CTMS Working for You? Unify and Optimize Your Approach to Clinical Trials
Live Webcast: Wednesday, April 26 at 1:00pm EDT
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Netherlands Company, OmniComm Collaborate

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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Improving Clinical Trial Transparency, Collaboration and Efficiencies
Live Webinar: Wednesday, March 29 at 11:00am EDT
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Updated for March, Business and People News

The latest updates to people moves and business news.


Take the Clinical Endpoints Adjudication Survey!

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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In this edition

A Look at Gottlieb as New FDA Commissioner
Updated for March, Business and People News
Leveraging Big Data for Site Selection

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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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Events

Imaging in Clinical Trials
3rd Annual Endpoint Adjudication
4th Annual eSource Data in Clinical Investigations Bootcamp
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Articles

Utilize the Cloud for Data-Intensive Research

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.


Leveraging Big Data for Site Selection

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.

Blog Posts

A Look at Gottlieb as New FDA Commissioner

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.


The Financial Case for Moving Away from Manual Processes

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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Ask the editor

Lisa Henderson
Editor in Chief
Lisa.Henderson@ubm.com

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Mike Tessalone
Publisher
Michael.Tessalone@ubm.com