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In this ISSUE

Virtual Clinical Trials: The Future of Patient Engagement?

Modeling and Simulation in Clinical Trials: Real Potential or Hype?

Gastroparesis Treatment: What’s Coming up Next

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Regulatory Authorities, EMA
Danger: EMA Reputation at Risk
As the EMA celebrates its 2017 highlights, the new year brings deeper challenges for the agency—including preserving the credibility of its patient-first mission.
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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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mHealth
Navigating the Use of Digital Health in Virtual Trials
In this interview, Dr. Michelle Longmire, CEO of Medable, will discuss her perspective on the advancements of digital health in clinical trials.
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Calendar
/ EFGCP Annual Conference 2018 2/20-2/21 /
/ Clinical Trial Budgeting & Forecasting 2/22 /
/ EU Clinical Trial Regulation Summit 3/06-3/07 /
/ ADF 2018 - Abuse Deterrent Formulations Summit 3/13-3/14 /
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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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Immuno-Gene Therapeutics in Hematological Cancers: How Science Drives Study Strategy
Live Webcast: Tuesday, February 20 at 11:00am EST
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Clinical Trial Future
The Future of Clinical Trial Modernization: What’s to Come in 2018
2017 has been an exciting year for the clinical trials industry on many fronts, driven by new methods, regulation, and technology, but what is to come in 2018?
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The Rare Disease Revolution
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Software and Services
Revolutionizing Clinical Trials Through Real-Time Data Capture and Analytics
This article discusses real-time data capture and analytics in clinical trials.
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Research Reveals a Need for Evolution in Randomization and Trial Supply Management (RTSM) Technology
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Analytical Model
Janssen Develops Analytical Vendor Oversight Model
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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Lisa Henderson
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Todd Baker
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