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In this ISSUE

European Pediatric Informed Consent and AF: Current Status of Country Requirements

GSK Addresses Clinical Outcomes Through Patient-Centric Studies

Building Blocks for Better Balance

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Click here and press play in our video player to watch a short video about Covance's Xcellerate Insights collaborative workspace, making sharing and information access among project teams easier, more secure, and more efficient.
Opinion
Is a Clinical Trial a Product or a Service?
Most people in our poll said it was a service, but others disagreed. Find out more in this follow-up from Michael Howley PA-C, PhD.
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Podcast: E-Signatures and Digital Workflows in Clinical Trials
In clinical trials, the use of eSignatures to improve document workflows such as protocols, informed consent, and investigator brochures, has increased. All documents that need signed approvals eSignatures can be implemented to streamline, improve and make the transferring of those documents more efficient. This podcast discusses areas in clinical trials where eSignatures and document workflow can be applied for upstream benefits. Click here to listen
Clinical Operations
5 Reasons it's Time for a Universal Standard of Knowledge in Clinical Research
Due to mistakes by research professionals, clinical trials have been subject to delays or even cancellations.
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Read this interview with IBM company (eClinical Division), discusses risk-based monitoring (RBM) and how the company is innovating a 25-year-old manual process to enable better monitoring decisions.
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Technology
Using Technology to Support NIH Policy
Industry professionals are searching for new technologies to support their trials following approval of an NIH policy supporting single IRB practices.
... /Read more/
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Drive better outcomes with improved trial design
Live Webinar: Tuesday, December 6 at 11am EST
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Simplifying the complexities of global rare disease drug development
On Demand
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Calendar
/ NORD 2016 Rare Diseases & Orphan Products Breakthrough Summit 10/17-10/18 /
Arlington, Virginia
/ IRT 2016 10/25-10/26 /
Philadelphia, Pennsylvania
/ Exploratory Clinical Development 10/26-10/27 /
Berlin, Germany
 
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Optimizing real-world evidence programs to generate value
Tailored approaches for emerging biopharma
On Demand
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New Approaches to Allergen Testing in Clinical Trials. Download your copy of the latest Clinical Insight from ACM Global Laboratories. Learn more
Risked-Based Monitoring
The Core of RBM is Centralized Monitoring
The use and awareness of risk-based monitoring is now impacting clinical trials of all sizes, indications and types as a core component more than ever before.
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Lisa Henderson
Editor in Chief
Lisa.Henderson@ubm.com
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Mike Tessalone
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Michael.Tessalone@ubm.com
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Continuous Glucose Monitoring (CGM) in Clinical Trials: An Evolving Regulatory Landscape
Live Webinar: Tuesday, October 25 at 2:00 PM EST
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Patient Centricity
What do Patients Want When Interacting with eDiaries? A 3-Part Series
Part 1 covers how sponsors can improve the study design and logistics of electronic diaries.
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Regulatory Changes in India and What It Means for Clinical Research in the Country
Live Webinar: Wednesday, October 19 at 11:00am EDT
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