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

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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Paper to eCOA: A Guide to Migration
Paper to eCOA: A Guide to Migration

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The Essential Guide to Electronic Informed Consent
The Essential Guide to Electronic Informed Consent