How Electronic Data Collection Helps Meet the FDA's Quality Guidelines

April 15, 2016

Offering guidance for generating strong evidence in clinical research, the acronym "ALCOA" is widely used to outline the FDA's fundamental elements of quality for clinical data. 

CRF Health VP of Quality Assurance, Bob Murray, details the individual components of ALCOA and describes how capturing clinical outcomes data electronically helps trial sponsors meet and exceed each guideline.

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eCOA Essentials: 1 Hour to Higher Quality Data
eCOA Essentials: 1 Hour to Higher Quality Data

<p>The industry's shift from paper to electronic Clinical Outcome Assessments (eCOA) in clinical trials is ...

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eCOA Design and Implementation Overview
eCOA Design and Implementation Overview