news roundup
Nominate a colleague with impressive leadership and career intentions—even yourself!—for Pharmaceutical Executive's 2018 Emerging Pharma Leaders Awards.
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High-efficacy Subgroups in Clinical Trials: Why They Matter and How to Find Them
Webinar Tuesday, June 26, 12-1pm ET
Ever wonder if a certain subgroup of patients might respond to your treatment better than others? Join this webinar to learn about SDC's novel method for identifying high-efficacy subgroups in clinical trials and how these subgroups can help optimize your clinical development strategy.
 Register now |
ERT introduced its advanced Trial Oversight solution, a performance and risk management application. This solution combines clinical and operational data in real-time to support complex clinical trials.
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Debunking the Myths of Risk-Based Monitoring for a New Approach to Quality Management
Thursday, June 28, 2018 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST
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Saama Technologies, Inc. announced the launch of a set of Artificial Intelligence capabilities DaLIA. This Deep Learning Intelligent Assistant will be used to solve clinical development pain points.
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Predicting Holistic Clinical Trial Cost Should Not Be A Struggle
Ying Jiang Explains What You Need To Know
Friday, June 22, 2018, 10am EDT
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ICON plc announced it has signed an agreement with AG Mednet to use Judi to manage workflow and ensure data quality for enhanced endpoint event adjudication services.
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FILLING THE GAPS IN SITE SELECTION
What You Don't Know Can Help You
Thursday, June 21, 2018 at 11:30am EDT
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Driving Product Development and Finding the Fast Track in Early-Phase Oncology Programs
Tuesday, June 19, 2018 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST
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Is RBM living up to the hype? The state of RBM in clinical development
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The Future of ECOA
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Articles
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.
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Functional Service Models Reimagined: Integrating services and innovation for accelerated clinical development
On Demand
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Companies can utilize the following five tools to set themselves up for a successful trial.
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Blog Posts
Peter O'Donnell explores the convergence of policy and science in new vaccine R&D pursuits in Europe.
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Design of Early Phase Clinical Trials: How to Increase Efficiency and Probability of Success?
On Demand
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In this article, we will discuss trends and challenges with medical monitoring clinical analytics, analyze the alignment of existing medical monitoring tools and technologies with ICH-E6 (R2) addendum guidelines, and discuss trends in medical monitoring insourcing and outsourcing models.
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