Presentations
21 CFR Part 312 vs the Reality of Clinical Trials
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21 CFR Part 312 vs the Reality of Clinical Trials
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We specialize in clinical data integrity audits. Unlike Computer System Validation consultants and system auditors, our comprehensive approach clearly identifies where your data integrity risks and issues are, links them to GCP regulatory requirements, and visually interprets them for easier understanding and communicating with your executive team or sponsors. Contact us for assistance with audits, mock inspections, remediation, or training for your promising staff. Read More