ACT

MARCH 19/2019

news roundup

People Moves and Business News

Please see the latest new hires and job changes, along with company milestone news.

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FDA's Acting Commissioner Named

Departing FDA Commissioner Gottlieb welcomed newly-named Acting Commissioner Norman (Ned) Sharpless, currently Director of the National Cancer Institute (NCI) at the National Institutes of Health (NIH), who will start next month.

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Technology: Friend vs Foe - Considerations for Practical Execution of a Risk-Based Monitoring Strategy
Tuesday, April 23, 2019 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST
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Envigo Offers New Solution to Enable FIH Studies

Envigo, a provider of non-clinical contract research services and research models, announced the launch of PATHWAY—an integrated solution that optimizes non-clinical safety assessment programs to enable first-in-human clinical trials.


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RBM Case Studies: How Artificial Intelligence and Machine Learning with Advanced Analytics are driving new levels of patient safety and study quality
Thursday, March 28, 2019 at 11am EDT
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Articles

Getting Serious About Plain Language Transparency

Ken Getz MBA, Director of Sponsored Research at the Tufts CSDD and Chairman of CISCRP, outlines the many barriers to delivering plain language clinical trial results summaries to study volunteers and the reasons why it is not embraced by the clinical research enterprise.


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Fast, Focused Medical Data Review – Use Cases by a Medical Monitor
Wednesday, March 27, 2019 at 11am EDT| 8am PDT| 3pm GMT| 4pm CET
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The Evolution of Patient Centricity

Regular contributor Moe Alsumidaie looks back over the coverage of patient centricity in Applied Clinical Trials to see how the initiative has progressed over the years.

In this edition

People Moves and Business News
FDA's Acting Commissioner Named
The Evolution of Patient Centricity

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Events

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Clinical Research as a Care Option
Clinical Trial Budgeting and Forecasting
5th Annual Endpoint Adjudication
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Blog Posts

How to Transition to RBM to Risk-Based Everything

As the industry moves to implement Risk-Based Everything (RBX)—a more holistic risk-based approach to quality management—targeted risk management, offers many benefits.


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Minimizing the Impact of Human Error, Subjectivity, and Labor Costs The Application of Digital Pathology in Clinical Trials
Tuesday, March 19, 2019 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET
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The Rise of Shared Digital Health Economy and Promise of Accelerated Clinical Research

Richard Tsai, Vice President of Marketing, Inspire discusses the growing number of collaborations among industry, academia, government, non-profit foundations, and patient advocacy organizations, specifically in the rare disease area of drug discovery and development.


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Lisa Henderson
Editor in Chief
LHenderson@mmhgroup.com

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Todd Baker
Group Publisher
TBaker@mmhgroup.com