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news roundup
The European Federation of Pharmaceutical Industries and Associations (EFPIA) has provided further evidence of the potential health risks posed by the upcoming relocation of the EMA.
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ERT Video Series
Check out the ERT video series, filmed on the show floor at DIA 2017, for interviews on Innovating Clinical Trial Management, eCOA in Clinical Research: Trends and Advances, and Optimizing Clinical Trial Imaging through Advanced Technology.
 Click here to watch all 10 short videos |
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The 2017 eClinical Landscape Study: Assessing Data Management Practices, Performance, and Challenges from the Tufts Center for the Study of Drug Development, reviews the state of data management in life sciences with an in-depth look at the insights and opinions of clinical data management professionals at more than 250 companies, including sponsors and CROs.
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Tomorrow's Clinical Trial, Powered by Modern EDC
See how to cut study build time in half, eliminate migrations, and remove the need for source data verification (SDV).
 See a preview and watch the full webinar here. |
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The considerable uncertainty caused by Brexit is proving a goldmine for conference organizers, it seems. The Drug Information Association (DIA) is the latest group to put together a meeting about this hot topic.
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Navigating the Regulatory Complexities of Orphan Drugs: Know the unwritten rules of designations and what's next
On Demand
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Bioclinica announced it has acquired Silicon Valley-based MDDX Research & Informatics, adding advanced cloud research image management and submission technologies to its extensive suite of eHealth solutions.
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Future-proofing your Pharmacovigilance Delivery Model: Achieving scalability and cost effectiveness with AI/smart machines
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Beyond #Buzzwords: How to deploy wearables and remote devices to transform your clinical trial execution
Live Webinar: Tuesday, December 5 at 11:00 am EST
 Register now |
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Rare Diseases and the Eye - Envisioning Strategies for Success
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Articles
Sponsors and CROs are looking into implementation of a Risk Based Monitoring approach to their clinical trials to achieve the objectives related to enhanced data quality, better monitoring of patient safety, and creating efficiencies in overall operations.
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RBM Technology Impact on Clinical Roles: Centralized Monitoring is streamlining activities and changing roles across clinical development
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ZS Associates specify the four pillars of patient centricity that can help the demands and complexities of clinical trials.
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Blog Posts
The operational subject of how the centralized authorization procedure is going to work when the UK is no longer part of the European Union is being discussed.
In this three-part blog series, we look at how electronic platforms can support and enhance data capture in several types of RWD programs: observational studies, pragmatic trials, and commercial programs.
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Oncology
The use of Natural History studies in order to examine a rare disease that will help facilitate drug development programs.
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CRF Health announced that its TrialMax Touch® solution has been selected for a landmark global oncology trial. The trial will involve more than 1,000 patients across 200 sites in 20 countries.
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