ACT

July 17/2018


news roundup

CluePoints Announces Partnership with ONO Pharmaceutical

CluePoints, a provider of RBM and Data Quality Oversight solutions, announces four year partnership with ONO Pharmaceutical. This agreement will see that ONO utilizes CluePoints centralized statistical monitoring platform in order to drive its RBM strategy and position in Japan.


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Debunking the Myths of Risk-Based Monitoring for a New Approach to Quality Management
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Synteract Acquires Dermatology Specialist CRO Cu-Tech

Synteract, a CRO providing full-service Phase I-IV clinical trials, has acquired Cu-Tech, a dermatology specialist CRO. With this acquirement, Synteract has created a dedicated center of dermatology development.


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Predicting Holistic Clinical Trial Cost Should Not Be A Struggle
Ying Jiang Explains What You Need To Know
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Clinerion and the P-HIS Development Group of Korea University Medical Center Collaborate

Clinerion has signed a Memorandum of Understanding with the P-HIS Development Group of Korea University Medical Center to support activities in developing a patient data platform in the Republic of Korea for precision medicine.


Policy and Practice Come Together on EU Vaccine Thrust

Peter O'Donnell explores the convergence of policy and science in new vaccine R&D pursuits in Europe.

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FILLING THE GAPS IN SITE SELECTION
What You Don't Know Can Help You
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In this edition

Policy and Practice Come Together on EU Vaccine Thrust
Five Steps to Making Your Clinical Trials Patient-Centric
Take two and Tweet me in the Morning: How Social Media is Reshaping Health Care

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Driving Product Development and Finding the Fast Track in Early-Phase Oncology Programs
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Events

Direct-to-Patient Clinical Trials
American Pharma Outsourcing Summit
Crossroads: An Artia Solutions Conference
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Articles

Five Steps to Making Your Clinical Trials Patient-Centric

Companies can utilize the following five tools to set themselves up for a successful trial.


Final Guidance on IRB Written Procedures Issued

The Office for Human Research Protections at the US Department of Health and Human Services and the US Food and Drug Administration issued a final guidance on May 17 on Institutional Review Board written procedures, which are required under both OHRP and FDA regulations.

Blog Posts

Take two and Tweet me in the Morning: How Social Media is Reshaping Health Care

Given the rapid changes in the communication landscape brought about by participative Internet use and social media, it is important to develop a better understanding of these technologies and their impact on health communication.


When is it Time to Kill Your Drug? Maybe Sooner Than You Think

Patients stand to lose the most when sponsors hold too tightly to drugs doomed to fail. This wastes precious time that patients don't have and squanders valuable resources.


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

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Todd Baker
Group Publisher
todd.baker@ubm.com