ACT

May 22/2018


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news roundup

Latest Business and People News

Updated employee announcements, business news, awards, and recognition in the industry today.


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Is RBM living up to the hype? The state of RBM in clinical development
Wednesday, June 13, 2018 at 11am EDT
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How Informed are your Participants?

RTI International addresses the challenge of clinical trial informed consent forms by teaming up with Consenter, a patient-engagement platform that solves the problem of clinical trial enrollment by combining communication science with digital, interactive technology.


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The Future of ECOA
Tuesday, June 12, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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Elligo Health Research Launches Research Ready Program

Elligo Health Research, a clinical research services provider, has launched a Research Ready program for physician practices interested in becoming a study site. This program expands and diversifies clinical trial patient populations because healthcare providers are now able to offer these studies to their patients as a care option.


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Functional Service Models Reimagined: Integrating services and innovation for accelerated clinical development
Wednesday, June 6, 2018 at 11am EDT
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Elsevier Study Probes How Animal Studies Predict Human Safety

Elsevier, global information analytics business, carried out an analysis of the ability of animal studies to predict human safety. The study examined the consistency between preclinical animal testing and observations made in human clinical trials.

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Design of Early Phase Clinical Trials: How to Increase Efficiency and Probability of Success?
Europe: Tuesday, June 5, 2018 at 3pm CEST | 2pm BST
North America: Thursday, June 14, 2018 at 11am EDT | 10am CDT | 8am PDT
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In this edition

Latest Business and People News
Maximizing Immuno-Oncology Clinical Trial Success
What's the EMA Worth?
CluePoints Launches Risk-Based Monitoring Starter Pack

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Protein Biotherapeutic BioAnalysis, by Immunoaffinity LC-MS: Latest Trends and Recommendations
On Demand
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Events

BIO International Convention
7th Annual Publication and Clinical Trial Transparency
American Pharma Outsourcing Summit
Crossroads: An Artia Solutions Conference
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Considerations when Addressing the Challenges of Time, Cost, and Data Standardization in Clinical Trials
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Articles

Master Protocols in Oncology: A Review of the Landscape

With technology's increasing ability to gather and analyze previously unmanageable data sets, and medicine's forays into genomics and targeted therapies, the time of the master protocol may be at hand.


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Operationalizing Gene Therapy Trials
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Maximizing Immuno-Oncology Clinical Trial Success

Examining the unique standards and related challenges when assessing the safety and efficacy of cancer immunotherapy candidates.


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Medicine Use and Spending in the U.S. A Review of 2017 and Outlook to 2022
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Blog Posts

Blockchain Concepts Emerge in Clinical Trials

In this interview, Munther Baara, Head of New Clinical Paradigms at Pfizer, will discuss his perspectives on how blockchain may impact clinical trials.


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Six Strategies for More Accurate Clinical Trial Forecasting & Budgeting
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What's the EMA Worth?

On Europe Day, the agency itself is right now keener than ever to assess its worth and the value of its services to Europe and to Europeans.


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Where Expertise Meets Nuance: Conducting PTSD Clinical Trials
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RBM

The Risk Based Monitoring Plan

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.

 

CluePoints Launches Risk-Based Monitoring Starter Pack

CluePoints has launched the "CluePoints RBM and ICH E6 (R2) Starter Pack" to help small and medium-sized enterprises achieve regulatory compliance through a "risk-based" approach.


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Ask the editor

Lisa Henderson
Editor in Chief
Lisa.Henderson@ubm.com

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Todd Baker
Group Publisher
todd.baker@ubm.com