Applied Clinical Trials Trends

In this ISSUE

FAQs for Immunotherapy Trials

Creating a Self-Sustaining Clinical Trial Quality Management System

Specialized Travel Services Can Help with Patient Retention

Patient Centricity

Remote Monitoring of Patients in Clinical Trials

Investment in mHealth and the adoption of wearables are significant initiatives that are changing the clinical trial process toward a more patient centered approach. These wearable technology initiatives have the potential to be the most innovative advances in drug development.
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Podcast: E-Signatures and Digital Workflows in Clinical Trials
In clinical trials, the use of eSignatures to improve document workflows such as protocols, informed consent, and investigator brochures, has increased. All documents that need signed approvals eSignatures can be implemented to streamline, improve and make the transferring of those documents more efficient. This podcast discusses areas in clinical trials where eSignatures and document workflow can be applied for upstream benefits.

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Clinical Operations

UCLA Studies Participant Payment

Patient drop out is a challenge that faces all clinical trials researchers as a number of reasons can contribute to patients failing to complete studies. UCLA conducted a trial to see if its mechanism for patient reimbursement was correlated with patient retention.
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Click here to watch a short video about Covance's Xcellerate Forecasting & Site Selection tool, which helps forecast study timelines and supports selection of optimal investigator sites.

Clinical Operations

Lean Outsourcing Models for Clinical Trials, Part 2: Optimizing Technology

A key success factor for lean models is the possession of technology that can measure performance and manage risk in a well-organized and user-friendly manner. This article describes the results of an investigation to identify and describe the basic requirements for such technology solutions.
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Read this interview with IBM company (eClinical Division), discusses risk-based monitoring (RBM) and how the company is innovating a 25-year-old manual process to enable better monitoring decisions.

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Simplifying the complexities of global rare disease drug development
On-Demand

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Calendar

/ Partnerships in Clinical Trials US /

Boston, Massachusetts

/ NORD 2016 Rare Diseases & Orphan Products Breakthrough Summit /

Arlington, Virginia

/ IRT 2016 /

Philadelphia, Pennsylvania

Optimizing real-world evidence programs to generate value
Tailored approaches for emerging biopharma
On-Demand

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Visit Capsugel at CPhI to learn more about our unique combination of science, engineering, formulation and capsule expertise.

For more information visit

Clinical Technology

Digital Transformation of SAE Data Capture in Clinical Studies

Processes for collecting data of serious adverse events (SAEs) and events of special interest (ESI) during clinical trials have been underwhelming for sponsors. Improving these processes using the latest digital advances can result in more complete analyses and more effective decision-making.
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Ask the editor

Lisa Henderson
Editor in Chief
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Mike Tessalone
Publisher
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Drive better outcomes with improved trial design
Live Webinar: Tuesday, December 6 at 11am EST

Regulatory Authorities

What Could Brexit Mean in Practice for Pharma?

Following the UK's decision to leave the European Union, the result has been uncertainty and speculation as pharma attempts to understand its implications. How this change will effect the pharma and life sciences industry as well as the European community remains to be seen.
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Regulatory Changes in India and What It Means for Clinical Research in the Country
Live Webinar: Wednesday, October 19 at 11:00am EDT

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