ACT

JUNE 11/2019


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news roundup

StudyKIK Joins SCRS

The Society for Clinical Research Sites has announced that StudyKIK has joined the organization as a Global Impact Partner. StudyKIK utilizes social media to provide patient recruitment solutions for clinical trial sites, CROs, and pharmaceutical companies.


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Real Patient Stories: The Trials of Finding Clinical Trials
For clinical trial sponsors, it can be frustrating trying to recruit participants for clinical trials. For patients, trying to find a clinical trial can be equally frustrating. Looking for studies online is like searching for a needle in a haystack. Patients and caregivers share their personal experiences in these candid interviews.
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Medidata Institute Will Provide Insights for Research Improvement

Medidata has launched its Medidata Institute. With industry partners, the aim is to deliver insights that redefine how technology, data, and artificial intelligence can fundamentally improve the way research is conducted. Initial partnerships of the Medidata Institute are with Castleman Disease Collaborative Network and Friends of Cancer Research.


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Operational Challenges in Resourcing and Executing Seasonal Infectious Diseases Studies
North America: Thursday, June 13, 2019 at 11am EDT | 10am CDT | 8am PDT
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Google Company Verily Partners with Pharma

Verily, an Alphabet company, has announced strategic alliances with Novartis, Otsuka, Pfizer Inc., and Sanofi to develop digitally innovative, patient-centered clinical research programs using Project Baseline's evidence generation platform and tools


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Operational Challenges in Resourcing and Executing Seasonal Infectious Diseases Studies
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Articles

Providing Oncology Trial Access to Rural Communities

With challenges in oncology trials, especially for rural communities and patient access, researchers must find efficient ways to tap smaller community treatment centers. One way to enhance the appeal of community treatment centers for clinical research is for these centers to join forces with larger companies, create a giant pool of patients and leverage technology.


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COPD – Tackling the Unmet Needs
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Tackling the Challenges of Transitioning Risk-Based Monitoring

Authors from Remarque Systems discuss how an RBM approach can help enhance the safety and efficiency of clinical trials.


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Refocusing on Risk Mitigation in Starting Clinical Trials
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In this edition

Tackling the Challenges of Transitioning Risk-Based Monitoring
Medidata Institute Will Provide Insights for Research Improvement
Walk for CISCRP's Medical Heroes at DIA

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A new way to assess changes in trial complexity, success and duration: The Clinical Development Productivity Index
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Challenges in Biosimilar Bioanalytical Assays and Sample Processing
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Events

Rare Disease Innovation and Partnering Summit
DIA 2019 Global Annual Meeting
Leadership for Drug Development Teams
Direct-to-Patient Trials
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Challenges in Biosimilar Bioanalytical Assays and Sample Processing
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Blog Posts

What's Next for Drug Validation in the Age of Precision Medicine?

The industry needs a faster, cheaper process to bring new therapies to more patients. Finding eligible patients quicker and collecting more data over longer periods is precisely what the digital health revolution is about.



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Ask the editor

Lisa Henderson
Editor in Chief
LHenderson@mmhgroup.com

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Todd Baker
Group Publisher
TBaker@mmhgroup.com