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news roundup
UPS announced a major expansion to its International Special Commodities program. Customers can ship biological substances, dangerous goods in excepted quantities, and shipments utilizing dry ice via UPS to more than 50 additional international destinations.
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Considerations for Efficient Site Contracts and Payments
Clinical trial agreement development has a tremendous impact on study start-up – integrating site-level budgets, payment terms, and Clinical Trial Management Systems set-up. By understanding the most important considerations for contract development and budget planning, you can execute a fully-integrated process that results in high-efficiency enabled contracts and payments.
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Medidata takes step to offer the most complete data and analytic capabilities in clinical research, with new predictive analytics and benchmarking in Edge Study Feasibility and MEDS Perform.
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Scientific Advice with Regulators – An Essential Tool in Early Drug Development
Live Webcast- Europe: Thursday, March 29, 2018 at 3:00pm CEST, North America: Tuesday, April 17 at 11:00am EDT
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TransCelerate BioPharma Inc., has unveiled a new global campaign called "One Person Closer" designed to help increase awareness of the growing need for clinical trial participants.
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The Benefits of a Data-driven Approach to Feasibility
Live Webcast: Tuesday, March 20 at 11:00am EDT
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Trial By Fire Solutions has expanded its SimpleTrials product, the first on-demand, subscription-based clinical trial management system.
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Immuno-Gene Therapeutics in Hematological Cancers: How Science Drives Study Strategy
Live Webcast: Tuesday, February 20 at 11:00am EST
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Articles
Case study shows that site activation is a key driver in determining patient enrollment cycle time, which can be minimized by identifying the "sweet spot" of sites to deploy for a clinical trial.
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The Rare Disease Revolution
On Demand
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This article discusses real-time data capture and analytics in clinical trials.
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Blog Posts
An industry shift has led toward more insourcing and in-house resources to run trials.
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Research Reveals a Need for Evolution in Randomization and Trial Supply Management (RTSM) Technology
On Demand
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Kristy Galante, Director Process and Infrastructure of External Alliances at Janssen, recently spoke about a novel vendor oversight model at ExL's 8th Clinical Quality Oversight Forum, and will expand on the model in this interview.
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Oncology
This eBook will focus on advancing research, drug development, and trial management in rare diseases. Articles cover considerations from virtual trials and eCOA to the case for highly-skilled CRAs.
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Due to a shifting landscape because of faster drug approvals, this article offers strategies for sponsors to design clinical trials.
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