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SEPTEMBER 12/2017


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news roundup

SGS Strengthens Early Phase Development Services

SGS clinical research announced it has consolidated its early phase drug development services into a single, comprehensive offering, primarily aimed at small and medium-sized biotechnology and spin-off companies.


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ERT Video Series
Check out the ERT video series, filmed on the show floor at DIA 2017, for interviews on Innovating Clinical Trial Management, eCOA in Clinical Research: Trends and Advances, and Optimizing Clinical Trial Imaging through Advanced Technology.
Click here to watch all 10 short videos


Parexel Expands Access Group for Real World Data

Parexel has developed a new dedicated real-world data service team with expertise in epidemiology, health economics and outcomes research, market access, analytics, medical sciences, and safety, as an expansion of its Access unit.


mProve, Greenphire Offer Patient Payment App

mProve Health a provider of mobile technologies for patient engagement and electronic clinical outcome assessments (eCOA), and Greenphire, a global clinical payment automation solutions provider, announced a partnership to provide patients with real-time access to ClinCard payment details via mProve's engagement app, mPal.


Alliance Established to Navigate UK Life Sciences

A group of life science service providers based in the United Kingdom have formed The Health Science Business Gateway (HSBG), an alliance that provides complete assistance for overseas companies which are looking to initiate business operations in the UK and navigate the life sciences landscape.

In this edition

Case Study for CRO Resource Management
A Review of ICH E6 R2
Parexel Expands Access Group for Real World Data
Oncology—Six Steps to Ensure Successful Clinical Trial Imaging

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Proactive Planning, a Transformational Revolution to Improving Clinical Trial Quality?
Live Webcast: Tuesday, September 26, 2017 at 1:00pm EDT
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Events

Real-World Evidence
Speed to IND for Biologics
IRT 2017
Risk-Based Trial Management and Monitoring
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Articles

Case Study for CRO Resource Management

This article reviews a recent FSP in which the client required a CRO to assume clinical monitoring and site support responsibility for more than 50 ongoing clinical trials across 45 countries, and launch new studies, while simultaneously reducing the client's annual operational spend by more than 20%.


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Clinical Trial Simulation: An Efficient Tool for Improved Study Designs, Dose Selection and Go/No-go Investment Decisions
Live Webcast: Tuesday, September 19 at 2:00pm BST and Thursday, September 28 at 10am EDT
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Make the Best of Enrollment Rescue Mode

This peer review article explores how sites tackle enrollment rescue situations, and provides some best practice considerations for how both sponsors and sites can make the most of these circumstances.

Blog Posts

A Review of ICH E6 R2

A recent roundtable highlights the main aspects of the guidelines, how organizations are responding to it, and the challenges they now face in an effort to achieve a common level of understanding across the organizations.


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Accelerate NASH Development: Next-generation Approaches to Overcome Recruitment and Study Execution Challenges
Live Webcast: Monday, September 18 at 11:00am EDT
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Finding Patients in Community Care Settings

This blog reviews AmerisourceBergen's recently launched AdvanceIQ Network, a network designed to match independent community oncology and urology practices with clinical trials and research opportunities.


Oncology

Six Steps to Ensure Successful Clinical Trial Imaging

With the importance of imaging in oncology trials, this article presents the rationale behind the utility of image analysis software and suggest best practices for sponsors looking to leverage this technology to ensure successful extraction of clinical trial imaging endpoints.


The Promise of Liquid Biopsy Technology

Liquid biopsies are aggressively addressing diagnostic barriers in oncology and may help to revolutionize cancer research, patient treatment and survivor care.

 

Mining Cancer Kryptonite in Historic Trial Data

Data sharing associated with cancer trials is beginning to lead to important new scientific insights. This is because for cancer trials, unlike trials for most other indications, the comparator arm used to evaluate the effectiveness of the experimental arm is not a placebo but is an active treatment (i.e., “standard of care”).

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Lisa Henderson
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Mike Tessalone
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